Primary Device ID | 00813830026931 |
NIH Device Record Key | fea371d2-e7c4-4a31-99bd-a0af578bde32 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pressure Relief |
Version Model Number | 22486-FRU |
Catalog Number | 22486-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 | 00813830026931 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-25 |
Device Publish Date | 2023-09-15 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRESSURE RELIEF 77794891 not registered Dead/Abandoned |
Lutin, Matthew R 2009-07-31 |
PRESSURE RELIEF 73225267 1149814 Dead/Cancelled |
W. R. Meadows, Inc. 1979-07-30 |
PRESSURE RELIEF 72297427 0873236 Dead/Expired |
W. R. MEADOWS, INC. 1968-05-06 |