Primary Device ID | 00880304848917 |
NIH Device Record Key | 668546af-f1a6-4464-980f-367237b54b97 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biomet Cannulated Screw System |
Version Model Number | SSI003514 |
Catalog Number | SSI003514 |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304848917 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304848917]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2016-12-22 |
00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
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