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G49d

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref LUTRONIC GENIUS

by Lutronic Corporation

Identity

Trade Name
G49D EUDAMED
N/A FDA UDI
Generic Name
Radio-frequency skin surface treatment system FDA UDI
Device Name
Electrosurgical Unit EUDAMED
G49D TIP(200, 0.5) Lutronic GENIUS (멸균) FDA UDI
Model / Reference
LUTRONIC GENIUS EUDAMED
G49D TIP(200, 0.5) Lutronic GENIUS FDA UDI
Description
G49D TIP(200, 0.5) Lutronic GENIUS (멸균) FDA UDI

Identifiers

Primary DI / UDI-DI
08809447652276 EUDAMEDFDA UDI
Basic UDI-DI
88094476511007AVT EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
Z12010902 ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE EUDAMED
GMDN Term
Radio-frequency skin surface treatment system FDA UDI

Classification

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

Yes

FDA UDI

Category: Foot-switch, electrical

G49d by Lutronic Corporation — Class IIb — MDR, 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/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
KR-MF-000009035
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 8396698f-24f8-453d-95b4-a646f8dd6ec4 61 fields · synced Jul 9, 2026
  • FDA UDI 727e9826-738a-40b0-b793-4dbdc2b9ba0c 35 fields · synced May 29, 2026