Primary Device ID | 00813830021134 |
NIH Device Record Key | b2a903c6-b339-4b4e-b42e-d7f44bac8d8a |
Commercial Distribution Discontinuation | 2016-09-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | FRU, Extension, Oxygen Liter/Flowmeter |
Version Model Number | 27429 |
Catalog Number | 27429 |
Company DUNS | 088302096 |
Company Name | ACCUTRON, 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 | false |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813830021134 [Primary] |
BZA | Connector, Airway (Extension) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
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