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AZUR Detachment Controller

FDA UDI

Class II (US FDA UDI)

by Microvention Inc.

Identity

Trade Name
AZUR Detachment Controller FDA UDI
Generic Name
Vascular implant detacher, electronic, single-use FDA UDI
Device Name
AZUR Detachment Controller FDA UDI
Model / Reference
45-4001-02 FDA UDI
Description
AZUR Detachment Controller FDA UDI

Identifiers

Catalog Number
45-4001 FDA UDI
Primary DI / UDI-DI
00840273201991 FDA UDI
FDA Product Code
KRD FDA UDI
GMDN Term
Vascular implant detacher, electronic, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Vascular implant detacher, electronic, single-use

AZUR Detachment Controller by Microvention Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular implant detacher, electronic, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microvention Inc.

Sources (1)

  • FDA UDI f17df65c-d8b5-4502-bc5f-17b4ea251cae 36 fields · synced Jun 8, 2026