MULTILOC 04019010S
GUDID H67904019010S0
TI MULTILOC END CAP F/MULTILOC NAIL/10MM EXTENSION-STERILE
SYNTHES (U.S.A.) LP
Bone nail end-cap| Primary Device ID | H67904019010S0 |
| NIH Device Record Key | e02da750-18df-4a64-a571-288e3cbf40b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MULTILOC |
| Version Model Number | 04.019.010S |
| Catalog Number | 04019010S |
| Company DUNS | 832637081 |
| Company Name | SYNTHES (U.S.A.) LP |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| 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 | |
| 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 | 10886982089595 [Primary] |
| HIBCC | H67904019010S0 [Secondary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K103002
FDA Product Code
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
[H67904019010S0]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-04-07 |
| Device Publish Date | 2015-09-14 |
On-Brand Devices [MULTILOC]
| H679SD030190060 | PERCUTANEOUS INSERTION HANDLE MULTILOC PROXIMAL HUMERUS NAIL |
| 07611819427235 | END CAP RULER F/MULTILOC HUMERAL NAILING SYSTEM |
| H679030190010 | RADIOGRAPHIC RULER FOR MULTILOC HUMERAL NAIL |
| H67904019015S0 | TI MULTILOC END CAP F/MULTILOC NAIL/15MM EXTENSION-STERILE |
| H67904019010S0 | TI MULTILOC END CAP F/MULTILOC NAIL/10MM EXTENSION-STERILE |
| H67904019005S0 | TI MULTILOC END CAP F/MULTILOC NAIL/5MM EXTENSION-STERILE |
| H67904019002S0 | TI MULTILOC END CAP F/MULTILOC NAIL/2MM EXTENSION-STERILE |
| H67904019000S0 | TI MULTILOC END CAP F/MULTILOC NAIL/0MM EXTENSION-STERILE |
Trademark Results [MULTILOC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTILOC 77965747 4071262 Live/Registered |
DEPUY SYNTHES, INC. 2010-03-23 |
 MULTILOC 74068999 1641981 Dead/Cancelled |
Precision Interconnect Corporation 1990-06-14 |
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