Primary Device ID | 10859290006301 |
NIH Device Record Key | 4e0a8d91-6ef4-4379-a2da-46ced8538e9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GAS SAMPLING LINE 120'x.050'x.108' M/F |
Version Model Number | 90151 |
Catalog Number | 90151 |
Company DUNS | 003530786 |
Company Name | TRUER MEDICAL, INC. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859290006304 [Primary] |
GS1 | 10859290006301 [Package] Contains: 00859290006304 Package: Carton [50 Units] In Commercial Distribution |
GS1 | 20859290006308 [Package] Contains: 00859290006304 Package: Carton [100 Units] In Commercial Distribution |
GS1 | 30859290006305 [Package] Package: Carton [8 Units] In Commercial Distribution |
BYX | Tubing, Pressure And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-08 |
Device Publish Date | 2022-06-30 |