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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

05-002 — Class I MDR by WUNDmed GmbH & Co. KG

MD Atlas
WUNDmed GmbH & Co. KG

EUDAMED last updated this device on Feb 1, 2022

05-002

426020662apf1F5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: WUNDmed GmbH & Co. KG
UDI-DI code: 04260206625841
Reference / catalog number: 05-002

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Manufacturer information

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

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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.

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: 04260206625841
Basic UDI-DI: 426020662apf1F5
Reference / catalog number: 05-002
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: 51
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)

M0599MEDICAL PLASTERS - 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
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Software identification