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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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RETI-port/scan 21 — 1 UDI-DI variant, MDD

MD Atlas
Roland Consult Stasche & Finger GmbH

Data from EUDAMED, last updated May 31, 2026

RETI-port/scan 21

B-04260157780279

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Roland Consult Stasche & Finger GmbH

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Device characteristics

Active device

Legacy certificates

Certificate number: DD601535220001
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-04260157780279
Device name: RETI-port/scan 21
Device model: gamma plus²
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Roland Consult Stasche & Finger GmbH
SRN: DE-MF-000021413
Country: Germany
Email: info@roland-consult.de
Phone: +49 3381 890 10 34

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSSBYBWH8Q51SFHSM6M6PJD5

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

04-99-3.2-JJ7XXX04260157780279