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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

2001485 — Class I MDR by etol Eberhard Tripp GmbH

MD Atlas
etol Eberhard Tripp GmbH

EUDAMED last updated this device on Jan 13, 2026

2001485

4007705doyenreinigerXT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: etol Eberhard Tripp GmbH
UDI-DI code: 04007705053023
Reference / catalog number: 2001485

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Manufacturer information

Organization name: etol Eberhard Tripp GmbH
SRN: DE-MF-000005599
Manufacturer status: Active

Related devices

20011484007705doyenreinigerXTOn the market 20055364007705doyenreinigerXTOn the market 20004724007705doyenreinigerXTOn the market 20014834007705doyenreinigerXTOn the market 20047824007705doyenreinigerXTOn 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.

Critical warnings

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

CW084
EUDAMED did not publish a description for this code.

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: 04007705053023
Basic UDI-DI: 4007705doyenreinigerXT
Reference / catalog number: 2001485
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)

V0799PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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
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Software identification