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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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Latex Classic — 4 UDI-DI variants, MDR (Albert Kerbl GmbH)

MD Atlas
Albert Kerbl GmbH

Data from EUDAMED, last updated May 23, 2026

Latex Classic

401865300344

4 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: Albert Kerbl GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 401865300344
Device name: Latex Classic
Device model: 15355-15358
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: Albert Kerbl GmbH
SRN: DE-MF-000007708
Country: Germany
Email: info@kerbl.com
Phone: +49 8086 933-100

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JSPXACDFETZRJZNH8HDN1S8Q

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

1535704018653074480
1535604018653074473
1535504018653074466
1535804018653153581