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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

A0000235 — Class IIa MDR by medentex GmbH

MD Atlas
medentex GmbH

EUDAMED last updated this device on Feb 2, 2026

A0000235

426071187-PureMotion-HZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: medentex GmbH
UDI-DI code: 04260711872358
Reference / catalog number: A0000235

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Manufacturer information

Organization name: medentex GmbH
SRN: DE-MF-000005860
Manufacturer status: Active

Related devices

A0000246426071187-PureMotion-HZOn the market A0000179426071187-PureMotion-HZOn the market A0000251426071187-PureMotion-HZOn the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW259
EUDAMED did not publish a description for this code.
CW258
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Netherlands		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260711872358
Basic UDI-DI: 426071187-PureMotion-HZ
Reference / catalog number: A0000235
Issuing entity: GS1

Classification

Risk category: Class IIa
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)

Z12119099VARIOUS DENTAL STOMATOLOGY INSTRUMENTS - 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
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

G10 111659 0001Issued
Quality management systemNotified body: 0123Expiry: Jun 29, 2026