Primary Device ID | 00887868263040 |
NIH Device Record Key | 2bab4532-f4ab-4388-b0ce-dfd3a6289550 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perfuse™ Decompression System |
Version Model Number | 800-0543 |
Catalog Number | 800-0543 |
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 | |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00887868263040 [Primary] |
FMF | Syringe, piston |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868263040]
Moist Heat or Steam Sterilization
[00887868263040]
Moist Heat or Steam Sterilization
[00887868263040]
Moist Heat or Steam Sterilization
[00887868263040]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-26 |
Device Publish Date | 2019-04-18 |
00887868263071 | 800-0546 |
00887868263064 | 800-0545 |
00887868263057 | 800-0544 |
00887868263040 | 800-0543 |
00887868263033 | 800-0542 |
00887868263026 | 800-0541 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERFUSE 86084745 not registered Dead/Abandoned |
Biomet Biologics, LLC 2013-10-07 |