Primary Device ID | 00887868099922 |
NIH Device Record Key | 2b51fa89-d9c9-4433-8314-560ec1078f31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PED. VHS VARI-ANGLE HIP SCREW |
Version Model Number | 200504 |
Catalog Number | 200504 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868099922 [Primary] |
KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00880304279803 | 200524 |
00880304279797 | 200523 |
00880304279780 | 200522 |
00880304279773 | 200521 |
00880304279766 | 200520 |
00880304279759 | 200519 |
00880304279742 | 200518 |
00880304279735 | 200517 |
00880304279728 | 200516 |
00880304279711 | 200515 |
00880304279704 | 200514 |
00880304279698 | 200513 |
00880304279681 | 200512 |
00880304279674 | 200511 |
00880304279667 | 200505 |
00880304279650 | 200503 |
00880304279643 | 200502 |
00880304279636 | 200501 |
00887868099922 | 200504 |