Trumpf

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: Trumpf FDA UDI
Generic Name: Surgical plume evacuation system FDA UDI
Device Name: Trumpf Medical Kit FDA UDI
Model / Reference: TRUMPFKIT02 FDA UDI
Description: Trumpf Medical Kit FDA UDI

Identifiers

Catalog Number: TRUMPFKIT02 FDA UDI
Primary DI / UDI-DI: 30845854081000 FDA UDI
FDA Product Code: FYD FDA UDI
GMDN Term: Surgical plume evacuation system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.5070 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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical plume evacuation system

Trumpf by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system.

MediMax Tech — MEDIMAX TECH INC. · Class II
Megadyne — Megadyne Medical Products, Inc. · Class II
Crystal Vision — I.C. Medical, Inc. · Class II
DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
Opaque ULPA Filter & Water Trap — I.C. Medical, Inc. · Class II
DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
ACU-EVAC — ACUDERM, INC. · Class II
MediSourceNet, Inc — Medisourcenet, 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: Conmed Corporation

Sources (1)

FDA UDI c207f608-3775-4f50-a064-3cfe76e0bf90 35 fields · synced May 31, 2026