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ArtiSential Electrodes, Monopolar Series (Hand-controlled)

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 5AMT01S-LH

by LivsMed Inc.

Identity

Trade Name
ArtiSential Electrodes, Monopolar Series (Hand-controlled) EUDAMED
Artisential Monopolar Spatula FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Laparoscopic Instruments - Electrodes EUDAMED
This product is sterile, single-use, invasive instrument that used in laparoscopic surgery. There are two version, one for Hook and Spatula. The two models are same except for end-tip. FDA UDI
Model / Reference
5AMT01S-LH EUDAMEDFDA UDI
Description
This product is sterile, single-use, invasive instrument that used in laparoscopic surgery. There are two version, one for Hook and Spatula. The two models are same except for end-tip. FDA UDI

Identifiers

Primary DI / UDI-DI
08800042703349 EUDAMEDFDA UDI
Basic UDI-DI
88000427MonopolarS8 EUDAMED
510(k) Number
K240657 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
K0201010302 LAPAR AND THORACOSCOPIC ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Germany 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5 Millimeter FDA UDI

ArtiSential Electrodes, Monopolar Series (Hand-controlled) by LivsMed Inc. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LivsMed Inc.
EUDAMED SRN
KR-MF-000011855
Authorised Representative
Meridius Medical Europe Limited IE-AR-000004258

Sources (2)

  • EUDAMED 1b4692e0-6add-43b0-9264-be6e9c5faf21 61 fields · synced Jun 18, 2026
  • FDA UDI 294680f4-ca12-47d8-bf58-9a2673c67d3a 37 fields · synced May 29, 2026