| Primary Device ID | 00880304608450 |
| NIH Device Record Key | dfa166ff-f1d8-43f7-820a-53470bf79766 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CINCH MODULAR ATTACHMENTS |
| Version Model Number | 31-555617 |
| Catalog Number | 31-555617 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304608450 [Primary] |
| HWI | CORKSCREW |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304608450]
Moist Heat or Steam Sterilization
[00880304608450]
Moist Heat or Steam Sterilization
[00880304608450]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-25 |
| Device Publish Date | 2020-05-15 |
| 00880304468658 | 31-555613 |
| 00880304468641 | 31-555618 |
| 00880304468481 | 31-555614 |
| 00880304464131 | 31-555612 |
| 00880304608450 | 31-555617 |
| 00880304608443 | 31-555615 |
| 00887868482854 | 31-555617 |
| 00887868482847 | 31-555616 |
| 00887868482830 | 31-555615 |
| 00887868482816 | 31-555613 |
| 00887868482793 | 31-555611 |
| 00887868482861 | 31-555618 |
| 00887868482809 | 31-555612 |