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Anastomosis Clip

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Anastomosis Clip FDA UDI
Generic Name
Surgical bulldog clamp, single-use FDA UDI
Device Name
Anastomosis Clip Sideward Bent 3mm LP FDA UDI
Model / Reference
07-096-17 FDA UDI
Description
Anastomosis Clip Sideward Bent 3mm LP FDA UDI

Identifiers

Catalog Number
07-096-17 FDA UDI
Primary DI / UDI-DI
04946329162233 FDA UDI
FDA Product Code
HBT FDA UDI
GMDN Term
Surgical bulldog clamp, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

Yes

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 — 7.9 Millimeter FDA UDI

Category: Surgical bulldog clamp, single-use

Anastomosis Clip by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI f74276aa-c711-431f-b9a7-392ebbbfd37b 36 fields · synced May 31, 2026