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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

171906 — Class I MDR by AKTORmed GmbH

MD Atlas
AKTORmed GmbH

EUDAMED last updated this device on Nov 3, 2025

171906

4260463840028V

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AKTORmed GmbH
UDI-DI code: 04260463849066
Reference / catalog number: 171906

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Manufacturer information

Organization name: AKTORmed GmbH
SRN: DE-MF-000006136
Manufacturer status: Active

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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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW999
Never use the ENDOFIX EXO if you detected any damage. Contact the corresponding service.
CW999
MEDICAL ELECTRICAL DEVICES are subject to special precautionary measures in regard to EMC. The ENDOFIX EXO may be installed and operated only in accordance with the EMC information contained in this manual.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04260463849066
Basic UDI-DI: 4260463840028V
Reference / catalog number: 171906
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: https://aktormed.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z129080VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - HARDWARE ACCESSORIES
Z12029080VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI-INVASIVE SURGERY - HARDWARE 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

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Expiration date
Manufacturing date
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Software identification