GLOBAL AP 213020000
GUDID 10603295090809
GLOBAL AP OSTEOTOME GUIDE PIN 3.2mm LONG
DEPUY ORTHOPAEDICS, INC.
Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable| Primary Device ID | 10603295090809 |
| NIH Device Record Key | 3e049e6d-eee5-45f4-8f98-1497fec627fc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GLOBAL AP |
| Version Model Number | 2130-20-000 |
| Catalog Number | 213020000 |
| Company DUNS | 080506581 |
| Company Name | DEPUY ORTHOPAEDICS, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10603295090809 [Primary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
[10603295090809]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-05-13 |
| Device Publish Date | 2018-06-15 |
On-Brand Devices [GLOBAL AP]
| 10603295090373 | GLOBAL AP FIXED ANGLE TAPER EXTRACTOR |
| 10603295090519 | GLOBAL AP BROACH / IMPLANT HANDLE |
| 10603295090960 | GLOBAL AP GENERAL CASE LID |
| 10603295090946 | GLOBAL AP GENERAL CASE & INSERTS |
| 10603295090915 | GLOBAL AP HUMERAL 2 CASE LID |
| 10603295090892 | GLOBAL AP HUMERAL 2 CASE & INSERT |
| 10603295090854 | GLOBAL AP HUMERAL 1 CASE LID |
| 10603295090830 | GLOBAL AP HUMERAL 1 CASE & INSERTS |
| 10603295091356 | GLOBAL AP HUMERAL HEAD ECC TRIAL 56 x 21 |
| 10603295091349 | GLOBAL AP HUMERAL HEAD ECC TRIAL 56 x 18 |
| 10603295091325 | GLOBAL AP HUMERAL HEAD TRIAL 56 x 21 |
| 10603295091301 | GLOBAL AP HUMERAL HEAD TRIAL 56 x 18 |
| 10603295091295 | GLOBAL AP HUMERAL HEAD ECC TRIAL 52 x 21 |
| 10603295091288 | GLOBAL AP HUMERAL HEAD ECC TRIAL 52 x 18 |
| 10603295091271 | GLOBAL AP HUMERAL HEAD ECC TRIAL 52 x 15 |
| 10603295091257 | GLOBAL AP HUMERAL HEAD TRIAL 52 x 21 |
| 10603295091233 | GLOBAL AP HUMERAL HEAD TRIAL 52 x 18 |
| 10603295091226 | GLOBAL AP HUMERAL HEAD TRIAL 52 x 15 |
| 10603295091219 | GLOBAL AP HUMERAL HEAD ECC TRIAL 48 x 21 |
| 10603295091202 | GLOBAL AP HUMERAL HEAD ECC TRIAL 48 x 18 |
| 10603295091196 | GLOBAL AP HUMERAL HEAD ECC TRIAL 48 x 15 |
| 10603295091172 | GLOBAL AP HUMERAL HEAD TRIAL 48 x 21 |
| 10603295091158 | GLOBAL AP HUMERAL HEAD TRIAL 48 x 18 |
| 10603295091141 | GLOBAL AP HUMERAL HEAD TRIAL 48 x 15 |
| 10603295091134 | GLOBAL AP HUMERAL HEAD ECC TRIAL 44 x 21 |
| 10603295091127 | GLOBAL AP HUMERAL HEAD ECC TRIAL 44 x 18 |
| 10603295091110 | GLOBAL AP HUMERAL HEAD ECC TRIAL 44 X 15 |
| 10603295091097 | GLOBAL AP HUMERAL HEAD TRIAL 44 x 21 |
| 10603295091073 | GLOBAL AP HUMERAL HEAD TRIAL 44 x 18 |
| 10603295091066 | GLOBAL AP HUMERAL HEAD TRIAL 44 X 15 |
| 10603295091059 | GLOBAL AP HUMERAL HEAD ECC TRIAL 40 X 18 |
| 10603295091042 | GLOBAL AP HUMERAL HEAD ECC TRIAL 40 X 15 |
| 10603295091035 | GLOBAL AP HUMERAL HEAD TRIAL 40 X 18 |
| 10603295091028 | GLOBAL AP HUMERAL HEAD TRIAL 40 X 15 |
| 10603295090786 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 16mm |
| 10603295090762 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 14mm |
| 10603295090748 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 12mm |
| 10603295090724 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 10mm |
| 10603295090700 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 8mm |
| 10603295090694 | GLOBAL AP HUMERAL STEM BROACH / TRIAL 6mm |
| 10603295090502 | GLOBAL AP BROACH HANDLE ADAPTOR |
| 10603295090380 | GLOBAL AP FIXED 135 TRIAL |
| 10603295005568 | GLOBAL AP REVISION STEM SIZE 14 217mm |
| 10603295005537 | GLOBAL AP REVISION STEM SIZE 12 217mm |
| 10603295005506 | GLOBAL AP REVISION STEM SIZE 10 207mm |
| 10603295005476 | GLOBAL AP REVISION STEM SIZE 8 197mm |
| 10603295090809 | GLOBAL AP OSTEOTOME GUIDE PIN 3.2mm LONG |
| 10603295090793 | GLOBAL AP OSTEOTOME GUIDE PIN 3.2mm SHORT |
| 10603295090571 | GLOBAL AP CALCAR ALIGNMENT GUIDE ASSEMBLY |
| 10603295090533 | GLOBAL AP ORIENTATION DEVICE ASSEMBLY |
Trademark Results [GLOBAL AP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 GLOBAL AP 78519191 3291583 Live/Registered |
DePuy, Inc. 2004-11-18 |
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