Primary Device ID | 00887868010002 |
NIH Device Record Key | c4f4174d-8758-4bd0-8b2a-54972c601a0f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CANNULATED CANCELLOUS S.C.F.E. SCREW |
Version Model Number | 14188-100 |
Catalog Number | 14188100 |
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 | false |
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 | 00887868010002 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868010002]
Moist Heat or Steam Sterilization
[00887868010002]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00887868010040 | 14188-120 |
00887868010033 | 14188-115 |
00887868010026 | 14188-110 |
00887868010019 | 14188-105 |
00887868010002 | 14188-100 |
00887868006463 | 14188-95 |
00887868006456 | 14188-90 |
00887868006449 | 14188-85 |
00887868006432 | 14188-80 |
00887868006425 | 14188-75 |
00887868006418 | 14188-70 |
00887868006401 | 14188-65 |
00887868006395 | 14188-60 |
00887868006388 | 14188-55 |
00887868006371 | 14188-50 |
00887868006364 | 14188-45 |
00887868006357 | 14188-40 |
00887868006340 | 14188-35 |
00887868006333 | 14188-30 |