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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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KENTAMED RF-120 — 2 UDI-DI variants, MDR (KENTAMED Ltd.)

MD Atlas
KENTAMED Ltd.

Data from EUDAMED, last updated May 23, 2026

KENTAMED RF-120

3800943RF120NJ

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: KENTAMED Ltd.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3800943RF120NJ
Device name: KENTAMED RF-120
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: KENTAMED Ltd.
SRN: BG-MF-000022619
Country: Bulgaria
Email: office@kentamed.com
Phone: +35932622934

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G5KF2NVYE8XK3ERP3YJN7PJ8

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

KENTAMED RF-12003800943000160
KENTAMED RF-120a03800943000184