Primary Device ID | 00889024187504 |
NIH Device Record Key | ac152d0d-7b1b-44f3-9746-89780454b766 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5220-54-04 |
Catalog Number | 00-5220-054-04 |
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 | 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)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com |
Height | 15 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024187504 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-31 |
Device Publish Date | 2015-09-24 |
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