Primary Device ID | 00812636022123 |
NIH Device Record Key | e84db610-cae1-46f7-8bd8-ab915e84f09a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroPearl |
Version Model Number | MP2S0100 |
Catalog Number | MP2S0100 |
Company DUNS | 003263105 |
Company Name | MICROVENTION INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
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 |
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 | 00812636022123 [Primary] |
KRD | Device, Vascular, for Promoting Embolization |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-07 |
Device Publish Date | 2018-08-07 |
00812636022147 | Bland Beads |
00812636022130 | Bland Beads |
00812636022123 | Bland Beads |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MICROPEARL 97701379 not registered Live/Pending |
Terumo Kabushiki Kaisha 2022-12-02 |
![]() MICROPEARL 97259185 not registered Live/Pending |
The Oncor Corp. 2022-02-09 |
![]() MICROPEARL 88568732 not registered Live/Pending |
Terumo Kabushiki Kaisha 2019-08-06 |
![]() MICROPEARL 86913486 not registered Dead/Abandoned |
Terumo Kabushiki Kaisha 2016-02-19 |
![]() MICROPEARL 74181827 1837584 Live/Registered |
SEKISUI KAGAKU KOGYO KABUSHIKI KAISHA 1991-07-02 |
![]() MICROPEARL 73316336 1248047 Live/Registered |
Matsumoto Yushi-Seiyaku Co., Ltd. 1981-06-25 |