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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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Kamerasysteme — 12 UDI-DI variants, MDR (Reinecker Vision GmbH)

MD Atlas
Reinecker Vision GmbH

Data from EUDAMED, last updated May 23, 2026

Kamerasysteme

42556338CAMUQ

12 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: Reinecker Vision GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42556338CAMUQ
Device name: Kamerasysteme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Reinecker Vision GmbH
SRN: DE-MF-000025998
Country: Germany
Email: info@reineckervision.de
Phone: +49625793110

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHYCJ20FHWH34TE7Z646KDS4

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

TOCA2K0104255633800305
TOCA2K1104255633800596
TOFL2K0204255633800312
TOFL2K0304255633800329
TOFL2K3104255633800602
TOPMIN0104255633800565
TOPMILI104255633800572
Topopad104255633800619
TOSMA2K104255633800299
TOPOTAB204255633800268
TOPOTAB304255633800275
TOPOTAB404255633800282