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Remote control robot-assisted endoscopic surgery instruments - hardware accessories in EUDAMED

Browse medical devices in the “Remote control robot-assisted endoscopic surgery instruments - hardware accessories” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.

Regulation & class

MDRMedical Device Regulation — (EU) 2017/745

Class IClass IIaClass IIbClass III

IVDRIn Vitro Diagnostic Regulation — (EU) 2017/746

IVDR Class AIVDR Class BIVDR Class CIVDR Class D

MDD (legacy)Medical Device Directive — 93/42/EEC

Class IClass IIaClass IIbClass III

IVDD (legacy)In Vitro Diagnostic Directive — 98/79/EC

IVDD — GeneralIVDD — Annex II List AIVDD — Annex II List BIVDD — Self-testing

AIMDD (legacy)Active Implantable Directive — 90/385/EEC

Manufacturer country

AustriaBelgiumBulgariaCroatiaCyprusCzechiaDenmarkEstoniaFinlandFranceGermanyGreeceHungaryIcelandIrelandItalyLatviaLiechtensteinLithuaniaLuxembourgMaltaNetherlandsNorwayPolandPortugalRomaniaSlovakiaSloveniaSpainSwedenSwitzerlandUnited Kingdom

Market country

Available in

Issuing entity

GS1HIBCCEUDAMEDICCBBAIFA

Manual availability

Has user manualHas eIFU portalNo manual

Device characteristics

Sterile

A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.

View in glossary →

Single-use device

A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.

View in glossary →

Contains latex

A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.

View in glossary →

Direct marking

Sterilization

CMR substance

A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.

View in glossary →

Reprocessed single-use

Annex XVI applicable

OEM applicable

Implantable device

An implantable device is intended to be totally or partially introduced into the body and to remain there after the procedure.

View in glossary →

Reagent (IVD)

Medical domain

Administration, withdrawal & collectionCardiovascularSurgeryDentalDermatologyIn vitro diagnosticsVarious medical devicesGynaecology & obstetricsImaging & radiologyActive implantsNephrology & dialysisNeurologyOphthalmologyENT (ear, nose & throat)OrthopaedicsWound care & dressingsRespiratory & anaesthesiaUrologyOther

EMDN status

Last updated

AfterBefore

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66 medical devices in EUDAMED

Medical equipment, accessories, software and consumables › Instruments for functional explorations and therapeutic interventions › Endoscopic and minimally invasive surgery instruments › Remote control robotic endoscopic surgery instruments

This is a sub-category of Medical equipment, accessories, software and consumables in the EMDN nomenclature.

Browse all Medical equipment, accessories, software and consumables

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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Regulation & class

MDRMedical Device Regulation — (EU) 2017/745

Class IClass IIaClass IIbClass III

IVDRIn Vitro Diagnostic Regulation — (EU) 2017/746

IVDR Class AIVDR Class BIVDR Class CIVDR Class D

MDD (legacy)Medical Device Directive — 93/42/EEC

Class IClass IIaClass IIbClass III

IVDD (legacy)In Vitro Diagnostic Directive — 98/79/EC

IVDD — GeneralIVDD — Annex II List AIVDD — Annex II List BIVDD — Self-testing

AIMDD (legacy)Active Implantable Directive — 90/385/EEC

Manufacturer country

Market country

Available in

Issuing entity

GS1HIBCCEUDAMEDICCBBAIFA

Manual availability

Has user manualHas eIFU portalNo manual

Device characteristics

Sterile

A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.

View in glossary →

Single-use device

A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.

View in glossary →

Contains latex

A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.

View in glossary →

Direct marking

Sterilization

CMR substance

A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.

View in glossary →

Reprocessed single-use

Annex XVI applicable

OEM applicable

Implantable device

An implantable device is intended to be totally or partially introduced into the body and to remain there after the procedure.

View in glossary →

Reagent (IVD)

Medical domain

EMDN status

Last updated

AfterBefore

1 2 3 4

Results Found

66 devices match your query

1 / 4

FeaturedSchein Orthopädie Service KG

Largest device portfolio · 58,355 devices

Get featured

FeaturedSchein Orthopädie Service KG

Most devices on the market · 58,355 devices on the market

Get featured

Y-LINE

171895

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

TENSION SLEEVE D5

141365

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

JOYSTICK-RH-IIS

242696

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840038X

Organization name

AKTORmed GmbH

Multi-DOFPositioningStand

FH28AR

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

69213483FH28A0182

Organization name

Fengh Medical Co., Ltd.

SHURUI Tissue Forceps

SR-ENT-SP0808

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

ADAPTER-2

172088

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840038X

Organization name

AKTORmed GmbH

SHURUI Needle Driver

SR-ENT-SP0807

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

SHURUI Maryland Bipolar Forceps

SR-ENT-SP0802S

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

PROBE PIN

212518

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

JOINT

212482

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

Motorized Positioning System for Endoscopic Surgery

FH28AR

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

69213483FH28A0182

Organization name

Fengh Medical Co., Ltd.

FreeHand 2.1 Panorama

52400021

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

383008873ROBOTSYSTEMS01VH

Organization name

MediAkris, razvoj in proizvodnja medicinskih naprav, d.o.o.

ENDOSCOPE CLAMP

141363

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

JOYSTICK-LH-IIA

202428

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840038X

Organization name

AKTORmed GmbH

SHURUI Curved Bipolar Dissector

SR-ENT-SP0801

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

SHURUI Large Needle Driver

SR-ENT-SP0810S

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

STERILE SET IIS PU / 10 ea.

192289

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840128Y

Organization name

AKTORmed GmbH

SHURUI Monopolar Cautery Hook

SR-ENT-SP0805

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

TROLLEY

120874

On the market

Risk category

Class I

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4260463840018T

Organization name

AKTORmed GmbH

SHURUI Large Tissue Forceps

SR-ENT-SP0809

On the market

Risk category

Class IIb

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697419119Endo-systemE5

Organization name

Beijing Surgerii Robotics Company Limited

View in glossary →