Primary Device ID | 10709078013864 |
NIH Device Record Key | f913635f-d8c3-4817-a1de-99fd92a073aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anesthesia Circuit |
Version Model Number | 9391 |
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 | 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 | 00709078013867 [Primary] |
GS1 | 10709078013864 [Package] Contains: 00709078013867 Package: Case [20 Units] In Commercial Distribution |
CAH | Filter, Bacterial, Breathing-Circuit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-09 |
Device Publish Date | 2022-09-01 |
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