Primary Device ID | 00880304377028 |
NIH Device Record Key | 9fb53f18-47a2-4451-a2ed-08b4c48cc795 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INTEGRATED SHOULDER SYSTEM |
Version Model Number | 441000010 |
Catalog Number | 441000010 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00880304377028 [Primary] |
KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2015-11-03 |
00880304387478 | 490715125 |
00880304387461 | 490614125 |
00880304387454 | 490512125 |
00880304387447 | 490411125 |
00880304387430 | 490207125 |
00880304387423 | 490106125 |
00880304378209 | 450732051 |
00880304378186 | 450628049 |
00880304378179 | 450422045 |
00880304378155 | 450320043 |
00880304378117 | 450115038 |
00880304377028 | 441000010 |
00880304195912 | 10804 |
00880304195844 | 10801 |
00880304008755 | 490309125 |
00880304008748 | 450524047 |
00880304008731 | 450217041 |
00880304005136 | 10805 |
00880304004870 | 10803 |