Primary Device ID | 00887868106262 |
NIH Device Record Key | c759919e-fc4e-4105-a52e-425963fbf2c7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISION FOOTRING SYSTEM |
Version Model Number | 21430 |
Catalog Number | 21430 |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868106262 [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 |
00880304282780 | 21415 |
00887868106262 | 21430 |
00887868106255 | 21425 |
00887868106248 | 21395 |
00887868106231 | 21235 |
00888480222569 | 21446 |
00888480222507 | 21444 |
00888480222309 | 21442 |
00888480222224 | 21440 |
00888480222088 | 21410 |
00888480222040 | 21405 |
00888480222026 | 21400 |
00888480221524 | 21270 |
00888480221487 | 21260 |
00888480221395 | 21245 |
00888480221388 | 21244 |
00888480221371 | 21243 |
00888480221364 | 21242 |
00888480221357 | 21240 |
00888480221296 | 21225 |