Primary Device ID | 00813830023640 |
NIH Device Record Key | ee6129db-51df-443d-85ef-c18bc78dd7e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FRU, N2O E-Yoke (4 Cylinder) |
Version Model Number | 20097-FRU |
Catalog Number | 20097-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 | 00813830023640 [Primary] |
CAM | Yoke Assembly, Medical Gas |
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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