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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

UB1000605 — Class I MDR by Taumedit GmbH

MD Atlas
Taumedit GmbH

EUDAMED last updated this device on Apr 3, 2024

UB1000605

426065744umedicalcoverEN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Taumedit GmbH
UDI-DI code: 04260657440789
Reference / catalog number: UB1000605

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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

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

CW009
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.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260657440789
Basic UDI-DI: 426065744umedicalcoverEN
Reference / catalog number: UB1000605
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: 200
Additional product description: Unsterile Geräteabdeckung, Abdeckbeutel 100 x 60 cm, 50 µm, Bulk
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