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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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ipalat Hydro Med akut Lutschpastillen — 2 UDI-DI variants, MDR

MD Atlas
Dr. Pfleger Arzneimittel GmbH

Data from EUDAMED, last updated May 23, 2026

ipalat Hydro Med akut Lutschpastillen

PP22860LP191

2 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: Dr. Pfleger Arzneimittel GmbH

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UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01JENTG2S01Y982M6HVQKZKA2W

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

DE-0252111802829848
DE-0252111916469003

Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: PP22860LP191
Device name: ipalat Hydro Med akut Lutschpastillen
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 9, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr. Pfleger Arzneimittel GmbH
SRN: DE-MF-000010172
Country: Germany
Email: info@dr-pfleger.de
Phone: +49 951 6043 0

Variants by status