Primary Device ID | 00813830024050 |
NIH Device Record Key | bf40930f-9790-4355-880a-a8df9b7951de |
Commercial Distribution Discontinuation | 2099-04-12 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FRU, Downspout, White |
Version Model Number | 27760 |
Catalog Number | 27760 |
Company DUNS | 088302096 |
Company Name | ACCUTRON, 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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813830024050 [Primary] |
BSZ | Gas-Machine, Anesthesia |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-22 |
Device Publish Date | 2019-04-12 |
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