Primary Device ID | 00889024681927 |
NIH Device Record Key | 08e15b6c-b25d-4fcd-aa07-f631c7662a0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alliance |
Version Model Number | 110040236 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024681927 [Primary] |
KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024681927]
Moist Heat or Steam Sterilization
[00889024681927]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-14 |
Device Publish Date | 2025-08-06 |
00889024518063 | SSI004735 |
00889024518056 | SSI004734 |
00889024518049 | SSI004733 |
00889024518032 | SSI004732 |
00889024518025 | SSI004731 |
00889024518018 | SSI004730 |
00889024518001 | SSI004729 |
00889024517998 | SSI004680 |
00889024517981 | SSI004679 |
00889024517974 | SSI004678 |
00889024682047 | 110040476 |
00889024682030 | 110040237 |
00889024682016 | 110040439 |
00889024681996 | 110040339 |
00889024681972 | 110037010 |
00889024681927 | 110040236 |
00889024681903 | 110040444 |
00889024681897 | 110040235 |