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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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Hypromellose 0.3% Eye Drops — 2 UDI-DI variants, MDR

MD Atlas
Penta Arzneimittel GmbH

Data from EUDAMED, last updated May 31, 2026

Hypromellose 0.3% Eye Drops

426059553MP06UD01KF

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Penta Arzneimittel GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426059553MP06UD01KF
Device name: Hypromellose 0.3% Eye Drops
Device model: Moisturizing Eye Drops
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Penta Arzneimittel GmbH
SRN: DE-MF-000006565
Country: Germany
Email: info@penta-arzneimittel.de
Phone: +49 9435 307138

Variants by status

UDI-DI variants

2 UDI-DI variants

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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

746894214260595533182
687070914260595533175