Primary Device ID | 10709078011457 |
NIH Device Record Key | b2c504cf-9033-48ca-ab97-382eaa8b6e72 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cannula |
Version Model Number | 5312 |
Company DUNS | 092673953 |
Company Name | WESTMED, 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00709078011450 [Primary] |
GS1 | 10709078011457 [Package] Contains: 00709078011450 Package: Case [50 Units] In Commercial Distribution |
CAT | Cannula, Nasal, Oxygen |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |
10709078011457 | Adult Nasal Cannula W/ 7' KROT |
10709078010870 | CO2 Sampling Nasal Cannula, 15" |
10709078012775 | Cannula, Pediatric, Divided, CO2/O2 |
10709078012768 | Cannula, Pediatric, Divided, CO2/O2 |
10709078012751 | Cannula, Adult, Divided, CO2/O2 |
10709078012744 | Cannula, Adult, Divided, CO2/O2 |
10709078012706 | LoFlo Sample Line, Neo. Cannula |
10709078012683 | LoFlo Sample Line, Ped. Cannula |
10709078012669 | LoFlo Sample Line, Adult, Cannula |