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Organization name
UDI-DI code
Reference / catalog number

Carabiner — Class I MDR by Physiotechnik…

MD Atlas
Physiotechnik Schaffarik GmbH

EUDAMED last updated this device on Mar 28, 2025

Carabiner

912013895Karabiner9F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Physiotechnik Schaffarik GmbH
UDI-DI code: 09120138950044
Reference / catalog number: MK-001

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Manufacturer information

Organization name: Physiotechnik Schaffarik GmbH
SRN: AT-MF-000004592
Manufacturer status: Inactive

Critical warnings

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

CW010
Die Karabiner müssen so positioniert werden, dass keine Druckstellen entstehen können. The carabiners must be positioned so that no pressure points can arise.

Market distribution

Primary placement in Austria; available across 1 country total.

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

Device identification

Trade name: Carabiner
UDI-DI code: 09120138950044
Basic UDI-DI: 912013895Karabiner9F
Reference / catalog number: MK-001
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: Stainless steel carabiner with “Schaffarik Board” engraving
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y0580LEARNING AND TRAINING DEVICES - ACCESSORIES

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

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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.