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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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ROTOFIX 32 A (MD) — 2 UDI-DI variants, MDR (Andreas Hettich GmbH)

MD Atlas
Andreas Hettich GmbH

Data from EUDAMED, last updated May 23, 2026

ROTOFIX 32 A (MD)

040506740100259Y

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: Andreas Hettich GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 040506740100259Y
Device name: ROTOFIX 32 A (MD)
Device model: 1207
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Andreas Hettich GmbH
SRN: DE-MF-000010680
Country: Germany
Email: oskar.doering@hettichlab.com
Phone: +49 7461 705 1274

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKVKDW5HJV5T6WAC6R79A6ST

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

1207-0104050674098120
120704050674098113