← Back to catalogue

Sugita Aneurysm Clip

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
SUGITA ANEURYSM CLIP FDA UDI
Generic Name
Aneurysm clip FDA UDI
Device Name
TYPE: FENESTRATED LARGE, PERMANENT, No.41 RANGE: 95-135gf(0.93-1.32N) MATERIAL: ISO 5832-7/ASTM F1058G2 BLADE: L-SHAPED MAXIMUM OPENING: 8.0mm GRIP SURFACE: SERRATED FDA UDI
Model / Reference
07-940-41 FDA UDI
Description
TYPE: FENESTRATED LARGE, PERMANENT, No.41 RANGE: 95-135gf(0.93-1.32N) MATERIAL: ISO 5832-7/ASTM F1058G2 BLADE: L-SHAPED MAXIMUM OPENING: 8.0mm GRIP SURFACE: SERRATED FDA UDI

Identifiers

Catalog Number
07-940-41 FDA UDI
Primary DI / UDI-DI
04946329061062 FDA UDI
FDA Product Code
HCI FDA UDI
GMDN Term
Aneurysm clip 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

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 5 Millimeter FDA UDI

Category: Aneurysm clip

Sugita Aneurysm Clip by Mizuho Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneurysm clip.

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 63b3adcf-d5b3-40d5-9a45-bfe3822178d5 36 fields · synced May 30, 2026