Primary Device ID | 00810050861380 |
NIH Device Record Key | d7654d32-b805-418b-86b7-3f4f1b3a792c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Side Arch |
Version Model Number | 100-4279-CF2-03 |
Company DUNS | 556196210 |
Company Name | LIFEPORT, 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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810050861380 [Primary] |
FOX | Stand, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-09 |
Device Publish Date | 2021-07-01 |
00810050861380 | INSTALLATION, SIDE ARCH, PIAGGIO P180 |
00810050862653 | INSTALLATION - SIDE ARCH |