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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

200 222 — Class I MDR by Novo Klinik-Service GmbH

MD Atlas
Novo Klinik-Service GmbH

EUDAMED last updated this device on Jan 15, 2025

200 222

4260402642114X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Novo Klinik-Service GmbH
UDI-DI code: 04260402640952
Reference / catalog number: 200 222

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Manufacturer information

Organization name: Novo Klinik-Service GmbH
SRN: DE-MF-000005289
Manufacturer status: Active

Related devices

200 4444260402642114XOn the market 100 4444260402642114XOn the market 200 4434260402642114XOn the market 200 4474260402642114XOn the market 801 4474260402642114XOn 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.

CW007
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	Jan 1, 1989	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260402640952
Basic UDI-DI: 4260402642114X
Reference / catalog number: 200 222
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)

R01058099TRACHEOSTOMY AND LARYNGECTOMY CANNULAS - VARIOUS ACCESSORIES

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
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Software identification