Primary Device ID | 00880304204591 |
NIH Device Record Key | ea436159-042b-466a-8dbf-b943f9afb636 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COPELAND SHOULDER SYSTEM |
Version Model Number | 11-114621 |
Catalog Number | 11-114621 |
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 | 00880304204591 [Primary] |
HSD | PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC 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 |
00880304204829 | 11-114648 |
00880304204812 | 11-114647 |
00880304204805 | 11-114646 |
00880304204799 | 11-114645 |
00880304204782 | 11-114644 |
00880304204775 | 11-114643 |
00880304204768 | 11-114642 |
00880304204751 | 11-114641 |
00880304204669 | 11-114628 |
00880304204652 | 11-114627 |
00880304204645 | 11-114626 |
00880304204638 | 11-114625 |
00880304204621 | 11-114624 |
00880304204614 | 11-114623 |
00880304204607 | 11-114622 |
00880304204591 | 11-114621 |