Primary Device ID | 00889024639805 |
NIH Device Record Key | 0e78666e-c067-4080-8453-0f385ee0a3a9 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 32-8106-00-13 |
Catalog Number | 32-8106-000-13 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024639805 [Primary] |
JDC | PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-07 |
Device Publish Date | 2022-02-25 |
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