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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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Transurethral RF Ablation Applicator — 1 UDI-DI variant, MDD

MD Atlas
Medical Enterprises Europe B.V.

Data from EUDAMED, last updated May 31, 2026

Transurethral RF Ablation Applicator

B-07290010121014

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: Medical Enterprises Europe B.V.

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Device characteristics

Active deviceAdministers medicine

Legacy certificates

Certificate number: CE 687158
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: BSI Group The Netherlands B.V. (2797)
Validity: May 22, 2024

Identity & classification

Basic UDI-DI: B-07290010121014
Device name: Transurethral RF Ablation Applicator
Device model: LI932B
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medical Enterprises Europe B.V.
SRN: NL-MF-000019133
Country: Netherlands
Email: info@synergo-medical.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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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

Transurethral RF Ablation Applicator07290010121014