Primary Device ID | 05707480102976 |
NIH Device Record Key | b4fdab3d-b6b1-4be0-a90c-2d60bab194f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hyperinflation (AMBU) |
Version Model Number | 900 000 606 |
Company DUNS | 092673953 |
Company Name | WESTMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 | 05707480102976 [Package] Contains: 05707480103119 Package: [12 Units] In Commercial Distribution |
GS1 | 05707480103119 [Primary] |
BZR | Mixer, Breathing Gases, Anesthesia Inhalation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2015-10-24 |
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