Primary Device ID | 00887868076824 |
NIH Device Record Key | 44766cde-e4c8-4bce-ae0a-3e5f2401fe01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | A.L.P.S.MIS LOCKING CALCANEAL PLATE |
Version Model Number | 110016966 |
Catalog Number | 110016966 |
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 | 00887868076824 [Primary] |
HRS | Plate, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-02-17 |
Device Publish Date | 2020-02-07 |
00887868076916 | 110016975 |
00887868076909 | 110016974 |
00887868076893 | 110016973 |
00887868076886 | 110016972 |
00887868076879 | 110016971 |
00887868076862 | 110016970 |
00887868076855 | 110016969 |
00887868076848 | 110016968 |
00887868076831 | 110016967 |
00887868076824 | 110016966 |
00887868076527 | 110008287 |
00887868076510 | 110008285 |
00887868076503 | 110008283 |
00887868076497 | 110008281 |
00887868076480 | 110008279 |
00887868076473 | 110008277 |
00887868076466 | 110008275 |
00887868076459 | 110008273 |
00887868076442 | 110008271 |
00887868076435 | 110008269 |