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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

201 802 - Schwarz — Class I MDR by feela., Marco Winter,…

MD Atlas
feela., Marco Winter, e-Commerce

EUDAMED last updated this device on Nov 4, 2022

201 802 - Schwarz

47449994620180X2H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: feela., Marco Winter, e-Commerce
UDI-DI code: 04744999460136
Reference / catalog number: 201 802 - Schwarz

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Manufacturer information

Organization name: feela., Marco Winter, e-Commerce
SRN: DE-MF-000011263
Manufacturer status: Active

Related devices

Art. 201 804 - Dunkelgrau47449994620180X2HOn the market Art. 201 804 - Schwarz47449994620180X2HOn the market Art. 201 804 - Silber47449994620180X2HOn the market 202 209, 202 210, 202 2114744999462022X337On the market 202 209 - Dunkelgrau4744999462022X337On 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.

CW010
Instabile Frakturen im Wirbelsäulen- und Beckenbereich; Offene Wunden; Lymphatische Fußerkrankungen, sensorische und kritische Durchblutungsstörungen der versorgten Körperregion; PAVK; Krankheitsbilder, bei denen der behandelnde Arzt oder Therapeut von deren Anwendung abrät

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: 04744999460136
Basic UDI-DI: 47449994620180X2H
Reference / catalog number: 201 802 - Schwarz
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)

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS

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