Primary Device ID | 00887868445590 |
NIH Device Record Key | a88be338-e72c-46f4-8822-bee98353813f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | A.L.P.S.® FOOT |
Version Model Number | 8166-08-003 |
Catalog Number | 816608003 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868445590 [Primary] |
JDW | PIN, FIXATION, THREADED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-20 |
Device Publish Date | 2020-07-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() A.L.P.S. 86414170 not registered Dead/Abandoned |
Biomet C.V. 2014-10-03 |
![]() A.L.P.S. 86122580 4795950 Live/Registered |
Biomet C.V. 2013-11-19 |
![]() A.L.P.S. 85887976 not registered Dead/Abandoned |
Biomet C.V. 2013-03-27 |