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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

EB013 — Class I MDR by Tischner & Thomann GmbH

MD Atlas
Tischner & Thomann GmbH

EUDAMED last updated this device on Aug 8, 2022

EB013

426069255EB015W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tischner & Thomann GmbH
UDI-DI code: 42700010824660
Reference / catalog number: EB013

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Manufacturer information

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

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.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 42700010824660
Basic UDI-DI: 426069255EB015W
Reference / catalog number: EB013
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)

Y060615ELBOW ORTHOSES

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