USB Medical Delivery Foreceps

FDA UDI

Class I (US FDA UDI)

by Nikomed Usa Inc

Identity

Trade Name: USB Medical Delivery Foreceps FDA UDI
Generic Name: Clamp manipulation forceps FDA UDI
Device Name: HV Heart Retractor FDA UDI
Model / Reference: DF-101 FDA UDI
Description: HV Heart Retractor FDA UDI

Identifiers

Catalog Number: DF-101 FDA UDI
Primary DI / UDI-DI: 00853512006790 FDA UDI
FDA Product Code: GDJ FDA UDI
GMDN Term: Clamp manipulation forceps 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

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

Yes

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

Category: Clamp manipulation forceps

USB Medical Delivery Foreceps by Nikomed Usa Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Clamp manipulation forceps.

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Symmetry Surgical — SYMMETRY SURGICAL INC. · Class II
Symmetry Surgical — SYMMETRY SURGICAL INC. · Class I
SCHWERT — A. Schweickhardt GmbH & Co. KG · Class I
Symmetry JACOBSON — SYMMETRY SURGICAL INC. · Class II
Symmetry Classic® — SYMMETRY SURGICAL INC. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Nikomed Usa Inc

Sources (1)

FDA UDI 7e45f55f-38d4-43db-a3e5-92c23ae381ba 35 fields · synced May 30, 2026