Sugita Titanium Clip II Applier

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name: Sugita Titanium Clip II Applier FDA UDI
Generic Name: Aneurysm clip applier FDA UDI
Device Name: Sugita Titanium Clip II Applier, Sano All-Angle for Mini w/o Catches FDA UDI
Model / Reference: 17-013-20 FDA UDI
Description: Sugita Titanium Clip II Applier, Sano All-Angle for Mini w/o Catches FDA UDI

Identifiers

Catalog Number: 17-013-20 FDA UDI
Primary DI / UDI-DI: 04946329187922 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 209.0 Millimeter FDA UDI

Category: Aneurysm clip applier

The Sugita Titanium Clip II Applier is a reusable surgical instrument designed for the application or insertion of aneurysm clips in neurology, specifically for approximating the edges of the neck of an aneurysm or preventing bleeding from small individual blood vessels. This applier is a critical medical device that requires proper sterilization and labeling to ensure patient safety.

Similar devices

Also classified as Aneurysm clip applier.

LAZIC — Peter Lazic GmbH · Class II
LAZIC — Peter Lazic GmbH · Class II
LAZIC — Peter Lazic GmbH · Class II
LAZIC — Peter Lazic GmbH · Class II
AESCULAP — AESCULAP, INC. · Class II
AESCULAP — AESCULAP, INC. · Class II
LAZIC — Peter Lazic GmbH · Class II
NOIR — AESCULAP, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Mizuho Corporation

Sources (1)

FDA UDI 575cbf4b-e595-4c96-ae25-205ab2170ba8 36 fields · synced Jul 31, 2026