EUDAMED last updated this device on Jun 19, 2026

NASPAN PLATINUM KORREKTURSPANGE

PP09450.NASPAN.SPANGE.K42

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Eduard Gerlach GmbH
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: -
Reference / catalog number: NASPAN PLATINUM KORREKTURSPANGE

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

NASPAN PLATINUM KORREKTURSPANGE is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Eduard Gerlach GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: NASPAN PLATINUM KORREKTURSPANGE
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: -
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: PP09450.NASPAN.SPANGE.K42
Reference / catalog number: NASPAN PLATINUM KORREKTURSPANGE
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: IFA

Classification

MDR risk classes MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face. View in glossary →: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 5
Additional product description: The Naspan Platinum nail correction system is a self-regulating, one-piece orthonyxia brace designed for the treatment of curled and ingrown toenails. The corrective brace is made of hypoallergenic, resilient surgical steel.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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EMDN nomenclature code(s)

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

Z12139004PODOLOGICAL TREATMENT UNITS

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

Consult instructions for use

Compliance flags

Safety

Reprocessed single-use

Direct marking

Substances

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2026	Still on market

NASPAN PLATINUM KORREKTURSPANGE

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UDI-DI DataMatrix

EMDN nomenclature code(s)

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Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

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Manufacturer information

Certificates covering this device

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