Primary Device ID | 00815948023888 |
NIH Device Record Key | a36392a7-f033-46e5-9e2f-1e803f1224ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RED 68 |
Version Model Number | RED68-B |
Company DUNS | 191077671 |
Company Name | PENUMBRA, 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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815948023888 [Primary] |
NRY | Catheter, Thrombus Retriever |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-22 |
Device Publish Date | 2021-07-14 |
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