Primary Device ID | 70880304416733 |
NIH Device Record Key | 19dcd4fb-fe68-40a2-9bfe-e47c0f3e6f7c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RESORBABLE SCREW SYSTEM |
Version Model Number | 951548 |
Catalog Number | 951548 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 6 |
DM Exempt | false |
Pre-market Exempt | true |
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 | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304416734 [Primary] |
GS1 | 70880304416733 [Unit of Use] |
HXI | PASSER, WIRE, ORTHOPEDIC |
Steralize Prior To Use | true |
Device Is Sterile | false |
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
[70880304416733]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2020-05-20 |
00880304416246 | 950044 |
00880304416161 | 950025 |
00880304416154 | 950012 |
70880304416733 | 951548 |