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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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Dermatril 740 — 37 UDI-DI variants, MDR (Kächele-Cama-Latex GmbH )

MD Atlas
Kächele-Cama-Latex GmbH

Data from EUDAMED, last updated May 23, 2026

Dermatril 740

40081987401789750DV

37 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: Kächele-Cama-Latex GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40081987401789750DV
Device name: Dermatril 740
Device model: Einmaluntersuchungshandschuh
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2022

Manufacturer & authorised representative

Manufacturer

Name: Kächele-Cama-Latex GmbH
SRN: DE-MF-000005184
Country: Germany
Email: vertrieb@kcl.de
Phone: +496659 870

Variants by status

UDI-DI variants

37 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FRG5SZQ267Y6H5JPG8CNGDRA

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

074810082C04008198874805
074807082C04008198874874
074811082C04008198874812
074906081C04008198774969
074907081C04008198774976
074911081C04008198774914
074909081C04008198774990
074908081C04008198774983
075008081C04008198775089
075010081C04008198775003
075007081C04008198775072
075009081C04008198775096

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