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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

SKLB0501105 — Class I MDR by Taumedit GmbH

MD Atlas
Taumedit GmbH

EUDAMED last updated this device on May 6, 2026

SKLB0501105

426065744smedicalcoverC4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Taumedit GmbH
UDI-DI code: 04260657447740
Reference / catalog number: SKLB0501105

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Manufacturer information

Organization name: Taumedit GmbH
SRN: DE-MF-000006701
Manufacturer status: Active

Related devices

UB1001005426065744umedicalcoverENOn the market UB1001005K426065744umedicalcoverENOn the market SB1001005426065744smedicalcoverC4On the market UB1001205426065744umedicalcoverENOn the market SB1001455ST426065744smedicalcoverC4On 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

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW136
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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260657447740
Basic UDI-DI: 426065744smedicalcoverC4
Reference / catalog number: SKLB0501105
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: Steriler Klappenbeutel 50 x 110 mm + 60 mm Klappe für Remote Controler verschließbar durch Adhäsionsstreifen
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0399PROTECTION DEVICES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT PPE) - 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