Primary Device ID | 00842429114360 |
NIH Device Record Key | 65c2f6c4-d15e-401c-87e2-77b2d727ad93 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stent |
Version Model Number | FREDX4023-PMA |
Catalog Number | FREDX4023 |
Company DUNS | 003263105 |
Company Name | MICROVENTION INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842429114360 [Primary] |
OUT | Intracranial aneurysm flow diverter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-10-10 |
Device Publish Date | 2022-04-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STENT 79230782 not registered Dead/Abandoned |
Air Bag Stopper Holdings Limited 2018-01-18 |