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Sugita Clip Applier

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Sugita Clip Applier FDA UDI
Generic Name
Aneurysm clip applier FDA UDI
Device Name
Sugita Clip Applier, Straight 21.5cm Length for Standard / Large Clips FDA UDI
Model / Reference
07-941-60 FDA UDI
Description
Sugita Clip Applier, Straight 21.5cm Length for Standard / Large Clips FDA UDI

Identifiers

Catalog Number
07-941-60 FDA UDI
Primary DI / UDI-DI
04946329061741 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 — 224.0 Millimeter FDA UDI

Category: Aneurysm clip applier

Sugita Clip 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 fba04d1a-bade-4b3c-b879-af51e5352895 36 fields · synced Jun 8, 2026