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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 50PLUS — 35 UDI-DI variants, MDR (Bingold GmbH + Co. KG)

MD Atlas
Bingold GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Latex 50PLUS

4004034LOC50G7

35 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: 4004034LOC50G7
Device name: Latex 50PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 15, 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

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FY6Y5QBY7XXN909C0HW12NV5

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

15072904004034004481
15065004004034004429
15072904004034006447
15073604004034006478
15071904004034006416
15065004004034006386
0888000904004034000339
0888000804004034000315
0888000704004034000292
0888001004004034000346

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