← Back to catalogue

System 1200

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
SYSTEM 1200 FDA UDI
Generic Name
Surgical plume evacuation system filter FDA UDI
Device Name
SYSTEM 1200 "Y" SMARTFILTER FDA UDI
Model / Reference
60-8055-001 FDA UDI
Description
SYSTEM 1200 "Y" SMARTFILTER FDA UDI

Identifiers

Catalog Number
60-8055-001 FDA UDI
Primary DI / UDI-DI
30653405040822 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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 filter

System 1200 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 38aeb5a9-c80f-4eca-a85a-70b120a01421 35 fields · synced Jun 6, 2026