Fumovac

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: FUMOVAC FDA UDI
Generic Name: Surgical plume evacuation system tube FDA UDI
Device Name: FUMOVAC Speculum tube set, 2.44 m, sterile FDA UDI
Model / Reference: 57525334 FDA UDI
Description: FUMOVAC Speculum tube set, 2.44 m, sterile FDA UDI

Identifiers

Catalog Number: 57525334 FDA UDI
Primary DI / UDI-DI: 20845854061937 FDA UDI
FDA Product Code: GAZ FDA UDI
GMDN Term: Surgical plume evacuation system tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Surgical plume evacuation system tube

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

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Gynex — GYNEX CORPORATION · Class I
Smoke Tubing — I.C. Medical, Inc. · Class II
STERILE SURGICAL SCISSORS — Anhui Medfaith Medical Devices Co., Ltd. · Class I
Bovie — BOVIE MEDICAL CORPORATION · 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

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Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI cf3ef9b0-bbdb-4777-941f-9557232b298f 36 fields · synced May 30, 2026