| Primary Device ID | 00880304251625 |
| NIH Device Record Key | 49dfd4a8-8568-42cc-8e67-7c0bb23d05cc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REACH REVISION HIP SYSTEM |
| Version Model Number | 162119 |
| Catalog Number | 162119 |
| 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 | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304251625 [Primary] |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00880304251632 | 162120 |
| 00880304251625 | 162119 |
| 00880304251618 | 162118 |
| 00880304251601 | 162117 |
| 00880304251595 | 162116 |
| 00880304251588 | 162115 |
| 00880304251571 | 162114 |
| 00880304251557 | 162113 |
| 00880304251540 | 162112 |
| 00880304251533 | 162111 |
| 00880304222632 | 12-162119 |
| 00880304222625 | 12-162117 |
| 00880304222618 | 12-162115 |
| 00880304222601 | 12-162113 |
| 00880304222595 | 12-162111 |
| 00880304208506 | 11-162120 |
| 00880304208490 | 11-162116 |
| 00880304208483 | 11-162115 |
| 00880304208476 | 11-162114 |
| 00880304208452 | 11-162113 |
| 00880304208445 | 11-162112 |
| 00880304208438 | 11-162111 |
| 00880304007871 | 11-162119 |
| 00880304007864 | 11-162117 |
| 00880304000575 | 11-162118 |