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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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RF300 — 1 UDI-DI variant, MDD

MD Atlas
Engineering Production Equipment Medical Srl

Data from EUDAMED, last updated May 30, 2026

RF300

B-8050714530005V8

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Engineering Production Equipment Medical Srl

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Device characteristics

Active device

Legacy certificates

Certificate number: ECM18MDD001
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ENTE CERTIFICAZIONE MACCHINE SRL (1282)
Validity: Feb 12, 2022

Identity & classification

Basic UDI-DI: B-8050714530005V8
Device name: RF300
Device model: Elettrobisturi
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Dec 14, 2021

Manufacturer & authorised representative

Manufacturer

Name: Engineering Production Equipment Medical Srl
SRN: IT-MF-000017628
Country: Italy
Email: epem@epem.net
Phone: +39 055331412

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FPWHB9ZX0AF82VCK67JF2JDR

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

RF300D-8050714530005V8