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CONMED Buffalo Filter

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED Buffalo Filter FDA UDI
Generic Name
Surgical plume evacuation system tube FDA UDI
Device Name
EY Tubing Kit 1-3/8 in (35 mm) x 6 ft (1.8 m) tube and six 2 ft (.6 m) tubes with integral wand & sponge guard FDA UDI
Model / Reference
VTEYKIT FDA UDI
Description
EY Tubing Kit 1-3/8 in (35 mm) x 6 ft (1.8 m) tube and six 2 ft (.6 m) tubes with integral wand & sponge guard FDA UDI

Identifiers

Catalog Number
VTEYKIT FDA UDI
Primary DI / UDI-DI
30845854061767 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Category: Surgical plume evacuation system tube

CONMED Buffalo Filter by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 95fcafe0-24d9-4cdc-82ec-38220f05c608 35 fields · synced Jun 8, 2026