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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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Organization name
UDI-DI code
Reference / catalog number

DBP-001 — Class I MDR by MED EUROPE EUROPEAN…

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

EUDAMED last updated this device on Dec 5, 2025

DBP-001

803360952ACCESSORI-DRENNK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
UDI-DI code: 08033609522026
Reference / catalog number: DBP-001

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Manufacturer information

Organization name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
SRN: IT-MF-000026962
Manufacturer status: Active

Related devices

PD-DS-2015803360952CANNULEG9On the market SIM 1-150cc803360952ACCESSORI-DRENNKOn the market MED ST-32 PVCB-08033609525126On the market TRACHEA SUCTION SET803360952ACCESSORI-DRENNKOn the market PAC 3.4 B-08033609524877On the market

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08033609522026
Basic UDI-DI: 803360952ACCESSORI-DRENNK
Reference / catalog number: DBP-001
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Low vacuum drainage system
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 500 MU48

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

A0680DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030102-00Issued
Quality management systemNotified body: 0425Expiry: Oct 17, 2029