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Organization name
UDI-DI code
Reference / catalog number

CBAS30200.3-01 — Class I MDR by Taumedit GmbH

MD Atlas
Taumedit GmbH

EUDAMED last updated this device on Jun 6, 2024

CBAS30200.3-01

426065744smedicalcoverC4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Taumedit GmbH
UDI-DI code: 04260657449577
Reference / catalog number: CBAS30200.3-01

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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

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.

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

Device identification

Trade name: not provided
UDI-DI code: 04260657449577
Basic UDI-DI: 426065744smedicalcoverC4
Reference / catalog number: CBAS30200.3-01
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: C-Bogen-Abdeckset 3 tlg. , 30 x 200 cm, mit 2 Abdeckbeutel 60 x 65 cm u. 90 x 75 cm steril, Set zur Geräteabdeckung gemeinsam in einem Klarsichtbeutel verpackt
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

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.