Primary Device ID | 00889024374898 |
NIH Device Record Key | 5cb18f38-9e33-4a08-89ca-05d31ee2d729 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 00-5049-088-00 |
Catalog Number | 00-5049-088-00 |
Company DUNS | 137354267 |
Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Serial Number | true |
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 |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024374898 [Primary] |
JDY | EVACUATOR, VAPOR, CEMENT MONOMER |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-18 |
Device Publish Date | 2019-03-08 |
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