Primary Device ID | 00813830028287 |
NIH Device Record Key | 7dc97d6f-7d15-40a4-b07e-e0e4a7540790 |
Commercial Distribution Discontinuation | 2099-02-15 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Oxygen Fitting, DISS with Female Q/C |
Version Model Number | 26849-FRU |
Catalog Number | 26849-FRU |
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 | 00813830028287 [Primary] |
BXY | Flowmeter, Calibration, Gas |
BYX | Tubing, Pressure And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-15 |
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