Primary Device ID | 10709078012454 |
NIH Device Record Key | a48c7758-9ca6-4fe8-9be0-0386adc9de2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aerosol Masks |
Version Model Number | 260-E |
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 | 00709078012457 [Primary] |
GS1 | 10709078012454 [Package] Contains: 00709078012457 Package: [50 Units] In Commercial Distribution |
BYG | Mask, 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 | 2021-01-08 |
Device Publish Date | 2020-12-31 |
10709078011426 | Pediatric Aerosol Mask w/ Vent Array |
10709078011419 | Adult Aerosol Mask w/ Vent Array |
10709078011402 | Aerosol Mask, Pediatric, Single Vents |
10709078012454 | Infant Aerosol Mask Single Vent |
10709078012447 | Aerosol Mask, Pediatric Elongated, Single Vents |