Primary Device ID | 00842429118795 |
NIH Device Record Key | 31e40341-64ee-43bf-925d-56c914c40cce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AZUR Detachment Controller |
Version Model Number | 45-4001-AL |
Catalog Number | 45-4001 |
Company DUNS | 003263105 |
Company Name | MICROVENTION INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | false |
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 |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 and 60 Degrees Celsius |
Storage Environment Humidity | Between 0 and 75 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842429118795 [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 | 2025-09-09 |
Device Publish Date | 2025-09-01 |
10810170012126 | Azur |
00840273201991 | AZUR Detachment Controller |
00842429118795 | AZUR Detachment Controller |