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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

MWR-P1 — Class I MDR by Angell Technology GmbH

MD Atlas
Angell Technology GmbH

EUDAMED last updated this device on May 14, 2024

MWR-P1

426246727WR-3D-001QH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Angell Technology GmbH
UDI-DI code: 42624672700011
Reference / catalog number: MWR-P1

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Manufacturer information

Organization name: Angell Technology GmbH
SRN: DE-MF-000041144
Manufacturer status: Active

Critical warnings

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

CW010
printed on packaging and type plate

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: 42624672700011
Basic UDI-DI: 426246727WR-3D-001QH
Reference / catalog number: MWR-P1
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: Weightbearing Radiography 3D-System
Additional information URL: https://angell-tech.com/service/download
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11079080VARIOUS SUPPORTING INSTRUMENTS FOR X-RAY FILM SYSTEM - 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.