Primary Device ID | 00887868053573 |
NIH Device Record Key | 57e7d831-cd51-4394-ad87-abe59da297db |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CANNULATED FULLY THREADED CANCELLOUS SCREW, REDUCED HEAD |
Version Model Number | 8502-48-046 |
Catalog Number | 850248046 |
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 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 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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868053573 [Primary] |
LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
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 |
00887868053634 | 8502-48-070 |
00887868053627 | 8502-48-065 |
00887868053610 | 8502-48-060 |
00887868053603 | 8502-48-055 |
00887868053597 | 8502-48-050 |
00887868053580 | 8502-48-048 |
00887868053573 | 8502-48-046 |
00887868053566 | 8502-48-044 |
00887868053559 | 8502-48-042 |
00887868053542 | 8502-48-040 |
00887868053535 | 8502-48-038 |
00887868053528 | 8502-48-036 |
00887868053511 | 8502-48-034 |
00887868053504 | 8502-48-032 |
00887868053498 | 8502-48-030 |
00887868053481 | 8502-48-028 |
00887868053474 | 8502-48-026 |
00887868053467 | 8502-48-024 |
00887868053450 | 8502-48-022 |
00887868053443 | 8502-48-020 |
00887868053436 | 8502-48-018 |
00887868053429 | 8502-48-016 |
00887868053412 | 8502-48-014 |
00887868053405 | 8502-48-012 |
00887868053399 | 8502-48-010 |