Primary Device ID | 00842429117798 |
NIH Device Record Key | d230cddd-afd8-4829-a2f6-7a77cd32d4ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stent |
Version Model Number | LEV3024-PMA |
Catalog Number | LEV3024 |
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 |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com |
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 | 00842429117798 [Primary] |
QCA | Intracranial coil-assist stent |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-04 |
Device Publish Date | 2023-04-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STENT 79230782 not registered Dead/Abandoned |
Air Bag Stopper Holdings Limited 2018-01-18 |