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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

ABPU02 — Class I MDR by Tischner & Thomann GmbH

MD Atlas
Tischner & Thomann GmbH

EUDAMED last updated this device on Apr 2, 2026

ABPU02

426069255ABPUA5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tischner & Thomann GmbH
UDI-DI code: 42606925591638
Reference / catalog number: ABPU02

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Manufacturer information

Organization name: Tischner & Thomann GmbH
SRN: DE-MF-000027113
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 42606925591638
Basic UDI-DI: 426069255ABPUA5
Reference / catalog number: ABPU02
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)

M030402010103ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN TWO DIRECTIONS, HIGH EXTENSIBILITY

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

Related devices

AB032426069255AB0152On the market AB031426069255AB0152On the market AB0112426069255AB0152On the market AB013426069255AB0152On the market AB012426069255AB0152On 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.