← Back to catalogue

Lumenis

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
LUMENIS FDA UDI
Generic Name
Surgical plume evacuation system filter FDA UDI
Device Name
FILTER/NON-STERILE TUBING FDA UDI
Model / Reference
LU0641-865 FDA UDI
Description
FILTER/NON-STERILE TUBING FDA UDI

Identifiers

Catalog Number
LU0641-865 FDA UDI
Primary DI / UDI-DI
20845854083328 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Surgical plume evacuation system filter 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

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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical plume evacuation system filter

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

Similar devices

Also classified as Surgical plume evacuation system filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI f938a05c-dd14-46d2-903b-f3ae43b25d1e 35 fields · synced Jun 8, 2026