Primary Device ID | 00880304251595 |
NIH Device Record Key | 30d86607-c8dd-428e-8324-2624f728c901 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REACH REVISION HIP SYSTEM |
Version Model Number | 162116 |
Catalog Number | 162116 |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304251595 [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 |