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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

SF-10-200-021-0060 — Class IIa MDR by ReDent Nova GmbH

MD Atlas
ReDent Nova GmbH

EUDAMED last updated this device on Nov 5, 2025

SF-10-200-021-0060

426235751SAF0012C

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ReDent Nova GmbH
UDI-DI code: 14262357510035
Reference / catalog number: SF-10-200-021-0060

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View device family (Basic UDI)

Manufacturer information

Organization name: ReDent Nova GmbH
SRN: DE-MF-000032545
Manufacturer status: Active

Related devices

SF-10-150-021-0057426235751SAF0012COn the market SF-10-150-025-0058426235751SAF0012COn the market B-SA-CRD-00-000-000-0890426235751CSM0013KOn the market B-SA-IMC-00-000-000-0784426235751MCD001Y3On the market B-SA-IMC-00-000-000-0839426235751MCD001Y3On 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

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

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 14262357510035
Basic UDI-DI: 426235751SAF0012C
Reference / catalog number: SF-10-200-021-0060
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Mechanically operated endodontic file to be used for cleaning and shaping of root canals
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2 MU50
21 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q010507ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE

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

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