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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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BL PRO-ACTIVE — 10 UDI-DI variants, MDR (Philipp Kirsch GmbH)

MD Atlas
Philipp Kirsch GmbH

Data from EUDAMED, last updated May 23, 2026

BL PRO-ACTIVE

426068858BLPROACTIVEF4

10 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Philipp Kirsch GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068858BLPROACTIVEF4
Device name: BL PRO-ACTIVE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Philipp Kirsch GmbH
SRN: DE-MF-000005605
Country: Germany
Email: luca.nollau@kirsch-medical.de
Phone: +49 781 9227 336

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHTKVA75HC3CS5CZE60WK2XA

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

1029704260688580010
1020004260688580003
1063604260688580034
1020104260688580027
1072604260688580058
1020904260688580041
1045304260688580096
1020204260688580089
1048504260688580133
1020604260688580126