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Sugita AVM Microclip Applier

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Sugita AVM Microclip Applier FDA UDI
Generic Name
Aneurysm clip applier FDA UDI
Device Name
Sugita AVM Microclip Applier short FDA UDI
Model / Reference
07-935-22-MA FDA UDI
Description
Sugita AVM Microclip Applier short FDA UDI

Identifiers

Catalog Number
07-935-22-MA FDA UDI
Primary DI / UDI-DI
04946329397888 FDA UDI
FDA Product Code
HCI FDA UDI
GMDN Term
Aneurysm clip applier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 165 Millimeter FDA UDI

Category: Aneurysm clip applier

Sugita AVM Microclip Applier by Mizuho Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneurysm clip applier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 14958d6f-3491-4006-92fc-adedf7b10457 36 fields · synced Jun 8, 2026