| Primary Device ID | 00887868055515 |
| NIH Device Record Key | 9d7e97f6-97fe-4435-9b36-b2e782070cc1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BAYONET TIP GUIDE WIRE |
| Version Model Number | 8514-17-960 |
| Catalog Number | 851417960 |
| 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 | 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868055515 [Primary] |
| FZX | Guide, surgical, instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-02-19 |
| Device Publish Date | 2020-05-23 |
| 00887868004087 - PRIMARY TREPHINE | 2024-04-03 |
| 00887868004094 - BUSHING | 2024-04-03 |
| 00887868004100 - SECONDARY TREPHINE | 2024-04-03 |
| 00887868048272 - TREPHINE | 2024-04-03 |
| 00887868048289 - TREPHINE | 2024-04-03 |
| 00887868048296 - TREPHINE | 2024-04-03 |
| 00887868048302 - TREPHINE | 2024-04-03 |
| 00880304658387 - Compress® | 2024-03-11 |