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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

350 500 — Class I MDR by mbnet Engineering GmbH

MD Atlas
mbnet Engineering GmbH

EUDAMED last updated this device on May 5, 2025

350 500

426071872handyvaqWC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: mbnet Engineering GmbH
UDI-DI code: 04260718720065
Reference / catalog number: 350 500

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Manufacturer information

Organization name: mbnet Engineering GmbH
SRN: DE-MF-000007410
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

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

CW014
EUDAMED did not publish a description for this code.
CW018
Refer to instruction manual/booklet: Consult instructions for use-(Description) See IFU for warnings, cautions, and instructions prior to using the device and for correct use of the device

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260718720065
Basic UDI-DI: 426071872handyvaqWC
Reference / catalog number: 350 500
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 117 MU50
78 MU50
27 MU50

EMDN nomenclature code(s)

C020599CARDIAC DIAGNOSTIC DEVICES - OTHER

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification