Primary Device ID | 00889024583283 |
NIH Device Record Key | 8a87f4fc-37b1-4684-a7d9-de2a65405db5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 8mm Narrow PPK Spacer Block |
Version Model Number | SSI005417 |
Catalog Number | SSI005417 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
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) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1 (800) 343-9500 |
customerservice@zimmerbiomet.com |
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 | 00889024583283 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
[00889024583283]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-02-11 |
Device Publish Date | 2020-02-03 |
00880304658387 - Compress® | 2024-03-11 |
08426750013848 - FRS™ SCREW | 2024-02-19 |
08426750013855 - FRS™ SCREW | 2024-02-19 |
08426750013862 - FRS™ SCREW | 2024-02-19 |
08426750013879 - FRS™ SCREW | 2024-02-19 |
08426750013886 - FRS™ SCREW | 2024-02-19 |
00887868455452 - K-Wire | 2024-02-19 |
00880304377868 - REUNITE PICK UPS | 2024-02-19 |