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Gomco Type Circumcision Clamp

FDA UDI

Class I (US FDA UDI)

by Fine Surgical Instruments Inc.

Identity

Trade Name
Gomco Type Circumcision Clamp FDA UDI
Generic Name
Circumcision clamp, reusable FDA UDI
Device Name
Gomco Type Circumcision Clamp Stainless Steel (German) XSML 1.1cm FDA UDI
Model / Reference
903-014 FDA UDI
Description
Gomco Type Circumcision Clamp Stainless Steel (German) XSML 1.1cm FDA UDI

Identifiers

Catalog Number
903-014 FDA UDI
Primary DI / UDI-DI
00869401000244 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Circumcision clamp, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

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 Unsafe FDA UDI

Category: Circumcision clamp, reusable

Gomco Type Circumcision Clamp by Fine Surgical Instruments Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Circumcision clamp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fine Surgical Instruments Inc.

Sources (1)

  • FDA UDI 11ab90a2-d803-4577-a2a6-99a48f8b9fe9 36 fields · synced May 31, 2026