Primary Device ID | 00840155411739 |
NIH Device Record Key | 1a087b6e-4d9a-4cc1-a462-e46ada40a0df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedSource Airway Devices |
Version Model Number | MS-238100 |
Catalog Number | Not Applicable |
Company DUNS | 041674552 |
Company Name | MEDSOURCE INTERNATIONAL LLC |
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 | 00840155411722 [Primary] |
GS1 | 00840155411739 [Package] Contains: 00840155411722 Package: Box [10 Units] In Commercial Distribution |
GS1 | 00840155411746 [Package] Contains: 00840155411722 Package: Case [200 Units] In Commercial Distribution |
CAE | Airway, Oropharyngeal, Anesthesiology |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-12-07 |
Device Publish Date | 2021-11-29 |
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