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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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DEBRICHEM — 1 UDI-DI variant, MDD (DEBx Medical BV)

MD Atlas
DEBx Medical BV

Data from EUDAMED, last updated May 30, 2026

DEBRICHEM

B-87202996029087Q

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: DEBx Medical BV

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: ECM21MDD003
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ENTE CERTIFICAZIONE MACCHINE SRL (1282)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-87202996029087Q
Device name: DEBRICHEM
Device model: DEBRICHEM 3ML
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: DEBx Medical BV
SRN: NL-MF-000010908
Country: Netherlands
Email: info@debx-medical.com
Phone: +31 085 0878096

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GBSGRZYVW4KA6RV7ZRJKC4VP

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

DMDD01D-87202996029087Q