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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

611 — Class I MDD by Ultratex GmbH

MD Atlas
Ultratex GmbH

EUDAMED last updated this device on Jan 22, 2025

611

B-04260739480047

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ultratex GmbH
UDI-DI code: 04260739480047
Reference / catalog number: 611

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Manufacturer information

Organization name: Ultratex GmbH
SRN: DE-MF-000005415
Manufacturer status: Active

Related devices

103-02426073948101B4On the market 103426073948101B4On the market 103-01426073948101B4On the market 102-03426073948101B4On the market 102-01426073948101B4On the market

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: 04260739480047
Basic UDI-DI: B-04260739480047
Reference / catalog number: 611
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Schutzhülle für Kalt- / Warmkompresse 260x430/470mm 500 Stück
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T030199COVERS, INSTRUMENTS AND EQUIPMENT - 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

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.