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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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Retractor System — 31 UDI-DI variants, MDR (Black Forest Medical GmbH)

MD Atlas
Black Forest Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Retractor System

42504355PA04EP

31 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Black Forest Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504355PA04EP
Device name: Retractor System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: Black Forest Medical GmbH
SRN: DE-MF-000005752
Country: Germany
Email: info@blackforestmedical.com
Phone: +4976138422210

Variants by status

UDI-DI variants

31 UDI-DI variants

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Applied filters

basicUdiUlid01KKC0TB1RTW2BEN44MY1P5THZ

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

3110-8004250435502662
3114-5404250435502891
1202.01404250435506479
1202.01504250435506509
1201.04504250435506363
1201.09104250435519196

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