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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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ALLERGIKA® sensitive Encasing — 74 UDI-DI variants, MDR

MD Atlas
ALLERGIKA Pharma GmbH

Data from EUDAMED, last updated May 23, 2026

ALLERGIKA® sensitive Encasing

PP1354514151654

74 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: ALLERGIKA Pharma GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP1354514151654
Device name: ALLERGIKA® sensitive Encasing
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: ALLERGIKA Pharma GmbH
SRN: DE-MF-000016908
Country: Germany
Email: michael.ernd@allergika.de
Phone: +49 8 171 42 25 7

Variants by status

UDI-DI variants

74 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J8HPYQ6FDPAPHXM9KVBVW93A

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

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1480111842980955
1411110192086601

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