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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 60PLUS — 5 UDI-DI variants, MDR (Bingold GmbH + Co. KG)

MD Atlas
Bingold GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Latex 60PLUS

4004034LOC60GA

5 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: Bingold GmbH + Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4004034LOC60GA
Device name: Latex 60PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: Bingold GmbH + Co. KG
SRN: DE-MF-000016561
Country: Germany
Email: info@bingold.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FY8SM1KNJNJXABFR3KD7DQ5V

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

213406804004034002968
213407104004034002906
213407004004034002876
213406904004034002845
213407204004034002937