← Back to catalogue

SUGITA AVM Microclip II CASE

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
SUGITA AVM Microclip II CASE FDA UDI
Generic Name
Surgical clip rack FDA UDI
Device Name
SUGITA AVM Microclip II CASE A FDA UDI
Model / Reference
07-932-10 FDA UDI
Description
SUGITA AVM Microclip II CASE A FDA UDI

Identifiers

Catalog Number
07-932-10 FDA UDI
Primary DI / UDI-DI
04946329389388 FDA UDI
FDA Product Code
HBR FDA UDI
GMDN Term
Surgical clip rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4215 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

Yes

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 — 252.4 Inch FDA UDI

Category: Surgical clip rack

SUGITA AVM Microclip II CASE by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical clip rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 418c0133-bb24-4a75-ad30-34817eaac08f 36 fields · synced May 30, 2026