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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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Hubtisch — 26 UDI-DI variants, MDR (OCULUS Optikgeräte GmbH)

MD Atlas
OCULUS Optikgeräte GmbH

Data from EUDAMED, last updated May 23, 2026

Hubtisch

404958422PT

26 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: OCULUS Optikgeräte GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 404958422PT
Device name: Hubtisch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: OCULUS Optikgeräte GmbH
SRN: DE-MF-000012227
Country: Germany
Email: sales@oculus.de
Phone: +49 641 2005 0

Variants by status

UDI-DI variants

26 UDI-DI variants

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Applied filters

basicUdiUlid01KPB0NENSM0QP8CTA4SYJ5SC3

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

Ophthalmic table04049584026392

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