EUDAMED last updated this device on Jul 30, 2026

TS181203

B-04260736210609

On the marketClass I

Applicable legislation: —
Organization name: Paul Schöndorf Metallwaren 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 →: 04260736210609
Reference / catalog number: TS181203

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.

TS181203 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Paul Schöndorf Metallwaren GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: not provided
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 →: 04260736210609
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 →: B-04260736210609
Reference / catalog number: TS181203
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 →: GS1

Classification

Risk category: Class I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Instrumenten-Sterilisierbehälter TS, L x B x H = 162 x 118 x 27 mm
Additional information URL: https://paulschoendorf.de/wp-content/uploads/2024/03/Instrumenten-Sterlisierbehaelter-TS_BA_DE.pdf
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

Encoded

(01)04260736210609

EMDN nomenclature code(s)

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

V0499CLINICAL USE CONTAINERS (NON-IVD) - OTHER

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	—	Still on market

TS181203

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Device details

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UDI-DI DataMatrix

EMDN nomenclature code(s)

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Regulatory

Lifecycle

Market distribution

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Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

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Safety

Regulatory

Lifecycle

Certificates

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