← Back to catalogue

Endopath

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 5DCD

by Ethicon Endo-Surgery, LLC

Identity

Trade Name
ENDOPATH EUDAMEDFDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
ENDOPATH Curved Monopolar Cautery Instruments EUDAMED
5 mm Curved Dissectors with Monopolar Cautery FDA UDI
Model / Reference
5DCD EUDAMEDFDA UDI
Description
5 mm Curved Dissectors with Monopolar Cautery FDA UDI

Identifiers

Catalog Number
5DCD FDA UDI
Primary DI / UDI-DI
10705036000778 EUDAMEDFDA UDI
Basic UDI-DI
0705036a000406J EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
K0201010202 LAPAROSCOPIC AND THORACOSCOPIC ELECTROSURGERY DISSECTORS, SINGLE-USE EUDAMED
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use 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

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Endopath by Ethicon Endo-Surgery, LLC — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000013107
Authorised Representative
Johnson & Johnson Medical GmbH DE-AR-000007712

Sources (2)

  • EUDAMED 1b43c9a4-c5de-4ba0-92ec-e4ed87f16e1f 61 fields · synced Jun 9, 2026
  • FDA UDI dc99ddb0-f814-4fa3-b7ee-df2813351641 36 fields · synced May 30, 2026