Primary Device ID | 00810050861519 |
NIH Device Record Key | 94dee265-2dae-4afe-b032-21d9c78015e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AeroSled Transport Deck (TD) |
Version Model Number | AS1-003-01 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810050861519 [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 | 2021-07-29 |
Device Publish Date | 2021-07-21 |
00810050861229 | AEROSLED TD, 37 INCH * BLUE |
00810050861373 | ASSEMBLY, AEROSLED TD |
00810050861434 | ASSEMBLY, AEROSLED TD |
00810050861427 | ASSEMBLY, AEROSLED TD |
00810050861519 | AEROSLED TD (200 LB) * TRANSPORT DECK, RED |
00810050861847 | AEROSLED, MACHINED, TD, 16G WITH LIMITATION PLACARD * TRANSPORT DECK |
00810050861892 | AEROSLED, 16G MA TD, 4IN CG LIMITATION PLACARD * TRANSPORT DECK |
00810050862806 | ASSEMBLY, AEROSLED TD, LOW G, WITH ROLLING FEET * RED |