| Primary Device ID | 00880304527454 |
| NIH Device Record Key | c1a29acc-5183-412a-824b-9dbaba25d3e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G7 ACETABULAR SCREW |
| Version Model Number | 010000997 |
| Catalog Number | 010000997 |
| 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 | 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 | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304527454 [Primary] |
| OQI | Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-11-29 |
| Device Publish Date | 2015-10-24 |
| 00880304527539 | 010001005 |
| 00880304527522 | 010001004 |
| 00880304527515 | 010001003 |
| 00880304527508 | 010001002 |
| 00880304527492 | 010001001 |
| 00880304527485 | 010001000 |
| 00880304527478 | 010000999 |
| 00880304527461 | 010000998 |
| 00880304527454 | 010000997 |
| 00880304527447 | 010000996 |