Primary Device ID | 00812636023519 |
NIH Device Record Key | dde4c91f-bec2-44d6-8588-7b64ae5cd9e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroPlex VFC |
Version Model Number | 8310-2060-A1 |
Catalog Number | 8310-2060 |
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 | 00812636023519 [Primary] |
KRD | Device, Vascular, for Promoting Embolization |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-11-21 |
Device Publish Date | 2016-09-24 |
00812636026237 | V-Trak |
00812636026220 | V-Trak |
00812636026190 | V-Trak |
00812636023519 | V-Trak |
00811425026212 | V-Trak |
00811425026205 | V-Trak |
00816777026279 | V-Trak |
00816777026262 | V-Trak |
00810170016271 | V-Trak |
00810170016264 | V-Trak |
00810170016257 | V-Trak |
00810170016233 | V-Trak |
00810170016226 | V-Trak |
00810170016219 | V-Trak |
00810170016202 | V-Trak |
00810170016196 | V-Trak |