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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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ANOKRYO — 3 UDI-DI variants, MDR (PakuMed medical products GmbH)

MD Atlas
PakuMed medical products GmbH

Data from EUDAMED, last updated May 31, 2026

ANOKRYO

426014678ANOKRYOJE

3 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: PakuMed medical products GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426014678ANOKRYOJE
Device name: ANOKRYO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: PakuMed medical products GmbH
SRN: DE-MF-000005123
Country: Germany
Email: info@pakumed.de
Phone: +49 201 4370970

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KPN37SRH9NRE5N915QBVGGGE

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

PZN 747015704260146783014
PZN 394153604260146783007
PZN 1907508704260146783021