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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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FROSTER BL PRO-ACTIVE — 9 UDI-DI variants, MDR (Philipp Kirsch GmbH)

MD Atlas
Philipp Kirsch GmbH

Data from EUDAMED, last updated May 23, 2026

FROSTER BL PRO-ACTIVE

426068858BLFROSTERPAJD

9 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: 426068858BLFROSTERPAJD
Device name: FROSTER 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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHTDSHFXS4DREPX80FNWWQ1Z

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

1023204260688580164
1023004260688580171
3533004260688580256
1023104260688580188
3553004260688580263
1023304260688580232
1022504260688580201
3573004260688580270
1023404260688580218