Vanguard SSI003729
GUDID 00889024517141
Zimmer, Inc.
Orthopaedic prosthesis implantation instrument, reusable| Primary Device ID | 00889024517141 |
| NIH Device Record Key | 8c3f5f17-325a-4416-8607-f3de85d9325b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vanguard |
| Version Model Number | SSI003729 |
| Catalog Number | SSI003729 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024517141 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
[00889024517141]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-28 |
| Device Publish Date | 2018-08-28 |
On-Brand Devices [Vanguard]
Trademark Results [Vanguard]
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