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System 5000

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 60-8015-SYSRef 60-8005-003Ref 60-8018-SYS

by Conmed Corporation

Identity

Trade Name
SYSTEM 5000 EUDAMEDFDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Device Name
Non-orthopedic, Active, Electrosurgical Generator, General purpose, System 5000 EUDAMED
SYSTEM 5000 100 - 230 VAC 50/60 Hz Electrosurgical Unit FDA UDI
THE SYSTEM 5000 - FULL SYSTEM 100 - 230 VAC 50/60 Hz Electrosurgical Unit FDA UDI
Model / Reference
60-8015-SYS EUDAMEDFDA UDI
60-8005-003 EUDAMEDFDA UDI
60-8018-SYS EUDAMEDFDA UDI
Description
SYSTEM 5000 100 - 230 VAC 50/60 Hz Electrosurgical Unit FDA UDI
THE SYSTEM 5000 - FULL SYSTEM 100 - 230 VAC 50/60 Hz Electrosurgical Unit FDA UDI

Identifiers

Catalog Number
60-8005-003 FDA UDI
60-8015-SYS FDA UDI
60-8018-SYS FDA UDI
Primary DI / UDI-DI
20653405040924 EUDAMEDFDA UDI
20653405040993 EUDAMEDFDA UDI
20653405040979 EUDAMEDFDA UDI
Basic UDI-DI
B-20653405040924 EUDAMED
B-20653405040993 EUDAMED
B-20653405040979 EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
Z12010902 ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE EUDAMED
GMDN Term
Electrosurgical system generator FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

System 5000 by Conmed Corporation — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation
EUDAMED SRN
US-MF-000012663
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (9)

  • EUDAMED 01e519ee-9e1b-4caf-b351-114408bb9f80 61 fields · synced Aug 4, 2026
  • EUDAMED 5fa002d7-a33d-4b1a-bba7-b68c8039fb20 61 fields · synced May 18, 2026
  • EUDAMED 68117ea1-03b8-498a-980a-86c7b8a20500 61 fields · synced May 18, 2026
  • FDA UDI 3dfa6162-df72-4693-8845-b95b355e770e 36 fields · synced May 30, 2026
  • FDA UDI d4781517-f70a-4e2d-ad7b-29ac8ca51e61 36 fields · synced May 30, 2026
  • FDA UDI 2e9a7734-1b6a-483c-9f61-3bdf4d9bfbd1 36 fields · synced May 30, 2026
  • EUDAMED 27112846-abc9-42b3-9632-ae22e50b0d4b 61 fields · synced Jul 23, 2026
  • EUDAMED 853b7072-b9bf-4d57-bde4-215db7789324 61 fields · synced Aug 4, 2026
  • EUDAMED a99aca82-c410-498e-8d6f-a38376916244 61 fields · synced Aug 4, 2026