Primary Device ID | 05019279131945 |
NIH Device Record Key | e50bdc5f-ceab-4edb-b89b-d330897e8be5 |
Commercial Distribution Discontinuation | 2019-12-19 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | AGC TOTAL KNEE INSTRUMENTATIONPREMIER CONTOUR BLOCK |
Version Model Number | 32-422383 |
Catalog Number | 32-422383 |
Company DUNS | 219322575 |
Company Name | Biomet Uk Ltd |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05019279131945 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
[05019279131945]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-12-20 |
Device Publish Date | 2017-10-09 |
05019279131952 | 32-422384 |
05019279131945 | 32-422383 |
05019279131938 | 32-422382 |
05019279131921 | 32-422381 |
05019279131914 | 32-401300 |