Primary Device ID | 00810170010262 |
NIH Device Record Key | fe97890b-c492-4dff-91ec-adcf57a2ccf8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroPlex HyperSoft Helical |
Version Model Number | 100201HS-V |
Catalog Number | 100201HS-V |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00810170010262 [Primary] |
HCG | DEVICE, NEUROVASCULAR 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 | 2018-12-21 |
Device Publish Date | 2018-11-20 |
00811425020296 | V-Trak |
00810170010408 | V-Trak |
00810170010392 | V-Trak |
00810170010385 | V-Trak |
00810170010378 | V-Trak |
00810170010361 | V-Trak |
00810170010354 | V-Trak |
00810170010347 | V-Trak |
00810170010330 | V-Trak |
00810170010323 | V-Trak |
00810170010316 | V-Trak |
00810170010309 | V-Trak |
00810170010286 | V-Trak |
00810170010262 | V-Trak |
04987350310279 | V-Trak |
00810170010279 | V-Trak |