VANGUARD 32-360081
GUDID 00880304496118
Biomet Orthopedics, LLC
Surgical flat-nosed pliers| Primary Device ID | 00880304496118 |
| NIH Device Record Key | 80db6fc4-ea9f-42d6-bea2-676cad34ac1b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VANGUARD |
| Version Model Number | 32-360081 |
| Catalog Number | 32-360081 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304496118 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K093293
FDA Product Code
| MBV | Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304496118]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
On-Brand Devices [VANGUARD]
Trademark Results [VANGUARD]
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