Primary Device ID | 00880304196667 |
NIH Device Record Key | 9be9500c-ea25-4373-b5a9-ae5093ec602e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REACH MODULAR HIP SYSTEM |
Version Model Number | 108391 |
Catalog Number | 108391 |
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 | 00880304196667 [Primary] |
MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
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 |
00880304282124 | 21-108399 |
00880304282117 | 21-108397 |
00880304282100 | 21-108393 |
00880304282094 | 21-108391 |
00880304282087 | 21-108293 |
00880304282070 | 21-108291 |
00880304196728 | 108401 |
00880304196711 | 108399 |
00880304196704 | 108397 |
00880304196681 | 108395 |
00880304196674 | 108393 |
00880304196667 | 108391 |
00880304196476 | 108301 |
00880304196452 | 108295 |
00880304196438 | 108293 |
00880304196421 | 108291 |
00880304009530 | 108299 |
00880304009035 | 21-108395 |
00880304007673 | 21-108297 |
00880304005662 | 21-108299 |
00880304003293 | 21-108295 |
00880304000131 | 108297 |