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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

04-037 — Class I MDR by WUNDmed GmbH & Co. KG

MD Atlas
WUNDmed GmbH & Co. KG

EUDAMED last updated this device on May 4, 2026

04-037

426020662wf9KP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: WUNDmed GmbH & Co. KG
UDI-DI code: 04260206624172
Reference / catalog number: 04-037

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Manufacturer information

Organization name: WUNDmed GmbH & Co. KG
SRN: DE-MF-000010322
Manufacturer status: Active

Related devices

02-128426020662kt3JROn the market 03-005426020662apf1F5On the market 02-105426020662apf1F5On the market 05-006426020662apf1F5On the market 05-007426020662apf1F5On the market

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

1 warning recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260206624172
Basic UDI-DI: 426020662wf9KP
Reference / catalog number: 04-037
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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