Primary Device ID | 00880304450172 |
NIH Device Record Key | 7866fa4d-12d0-4b78-ac47-dd8dc32093a7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REGENEREX HIP SYSTEM |
Version Model Number | PT-210356 |
Catalog Number | PT-210356 |
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 | 00880304450172 [Primary] |
KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
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 |
00880304453807 | PT-124252 |
00880304450257 | PT-210152 |
00880304450240 | PT-210154 |
00880304450233 | PT-210358 |
00880304450226 | PT-210156 |
00880304450219 | PT-210352 |
00880304450202 | PT-210354 |
00880304450196 | PT-210258 |
00880304450189 | PT-210256 |
00880304450172 | PT-210356 |
00880304450165 | PT-210252 |
00880304450158 | PT-210158 |
00880304450141 | PT-210254 |
00880304449350 | PT-126474 |
00880304449343 | PT-125060 |
00880304449336 | PT-124858 |
00880304449329 | PT-124454 |
00880304449312 | PT-125262 |
00880304449305 | PT-124656 |
00880304449299 | PT-125464 |
00880304449282 | PT-126676 |
00880304449275 | PT-125666 |
00880304449268 | PT-126070 |
00880304449251 | PT-126272 |
00880304449244 | PT-125868 |