Primary Device ID | 00810050862141 |
NIH Device Record Key | aea1c42e-8470-46aa-80c4-663d29156836 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Three Patient Litter System (TPLS) |
Version Model Number | 15-00266-02-P01-A01 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810050862141 [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 | 2022-08-24 |
Device Publish Date | 2022-08-16 |
00810050861137 | CONFIGURATION, THREE PATIENT LITTER SYSTEM (TPLS) * S-70i/M |
00810050862141 | CONFIGURATION, THREE PATIENT LITTER SYSTEM (TPLS) |