Primary Device ID | 00842636020577 |
NIH Device Record Key | c1002dc3-c3c3-4db6-96a6-704915cf7b23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Scepter C |
Version Model Number | BC0415C-B-ID |
Catalog Number | BC0415C |
Company DUNS | 003263105 |
Company Name | MICROVENTION INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 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 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 | 00842636020577 [Primary] |
DQY | CATHETER, PERCUTANEOUS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2020-01-13 |
Device Publish Date | 2016-09-24 |
00810170018558 | Balloon Catheter |
00810170018541 | Balloon Catheter |
00810170018534 | Balloon Catheter |
00810170015823 | Balloon Catheter |
00810170015816 | Balloon Catheter |
00810170015809 | Balloon Catheter |
00842636020584 | Balloon Catheter |
00842636020577 | Balloon Catheter |
00842636020560 | Balloon Catheter |
00842636020553 | Balloon Catheter |
00842636020546 | Balloon Catheter |
00842636020539 | Balloon Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SCEPTER C 85201027 4305692 Live/Registered |
MicroVention, Inc. 2010-12-17 |