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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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CHT-Spekula Set — 6 UDI-DI variants, MDR (HERRMANN Apparatebau GmbH)

MD Atlas
HERRMANN Apparatebau GmbH

Data from EUDAMED, last updated May 23, 2026

CHT-Spekula Set

4050417HAB-CHTa-D5

6 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: HERRMANN Apparatebau GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4050417HAB-CHTa-D5
Device name: CHT-Spekula Set
Device model: CHT-Spekula Set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: HERRMANN Apparatebau GmbH
SRN: DE-MF-000006133
Country: Germany
Email: info@hab.gmbh
Phone: +49 6 022 6581 3

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HWWNZRFEWDWZ9KJSA11F44VP

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

1780404050417178041
1780504050417178058
1780204050417178027
1780304050417178034
1780004050417178003
1780104050417178010