Primary Device ID | 00816777024152 |
NIH Device Record Key | 145b28a2-47f1-4dd2-9afe-9ad1ded3f876 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroPlex Cosmos |
Version Model Number | 100933CSSR-V |
Catalog Number | 100933CSSR-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 |
Phone | +1(714)247-8000 |
customerservice@microvention.c | |
Phone | +1(714)247-8000 |
customerservice@microvention.c | |
Phone | +1(714)247-8000 |
customerservice@microvention.c |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816777024152 [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 | 2018-09-07 |
Device Publish Date | 2018-08-07 |
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