Primary Device ID | 00842429106884 |
NIH Device Record Key | 89f361b2-f3b7-4168-b8c5-d92595e65a45 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Balloon Catheter |
Version Model Number | BC0410C-ID-2 |
Catalog Number | BC0410C |
Company DUNS | 003263105 |
Company Name | MICROVENTION 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 | 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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842429106884 [Primary] |
MJN | Catheter, intravascular occluding, temporary |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-30 |
Device Publish Date | 2025-04-22 |
00842429106563 | Scepter Mini |
00842429103418 | Scepter XC |
00842429103401 | Scepter C |
00842429103395 | Scepter C |
00842429103388 | Scepter C |
00842429106945 | Scepter XC |
00842429106907 | Scepter C |
00842429106891 | Scepter C |
00842429106884 | Scepter C |