FDA UDI In Commercial Distribution 🇺🇸 United States

Azur

DI: 00842429119150 · Model: 45-780204-02 · Microvention, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Azur
Primary DI
00842429119150
Version / Model
45-780204-02
Catalog Number
45-780204
Company Name
Microvention, Inc.
Labeler DUNS
003263105
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-25
Public Version
2
Public Version Date
2026-04-28
Public Version Status
Update
Public Device Record Key
91ffb091-d661-4155-a7d5-b70d48203cae

Device Description

Azur CX Detachable

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRD Device, Vascular, for Promoting Embolization

GMDN Terms

Code Name
60941 Non-neurovascular embolization coil

Identifiers

Type ID
Primary 00842429119150

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2 mm x 4 cm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry. Keep away from sunlight.