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Penis Clamp

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
PENIS CLAMP FDA UDI
Generic Name
Surgical penis clamp, single-use FDA UDI
Device Name
STOCKMAN (ZIPSER) PENIS CLAMP 5.5 INCH FDA UDI
Model / Reference
STOCKMAN (ZIPSER) PENIS CLAMP FDA UDI
Description
STOCKMAN (ZIPSER) PENIS CLAMP 5.5 INCH FDA UDI

Identifiers

Catalog Number
ZC110 FDA UDI
Primary DI / UDI-DI
B974ZC1100 FDA UDI
FDA Product Code
FHA FDA UDI
GMDN Term
Surgical penis clamp, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5160 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Surgical penis clamp, single-use

Penis Clamp by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical penis clamp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 426901d0-6306-44c4-a27e-91f3f699c0d3 35 fields · synced May 30, 2026