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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

Mirror plate for resi PRONE — Class I MDR by Anel AG

MD Atlas
Anel AG

EUDAMED last updated this device on Mar 13, 2026

Mirror plate for resi PRONE

764037203PFHT&PFMR83

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Anel AG
UDI-DI code: 07640372030262
Reference / catalog number: PFMR

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Manufacturer information

Organization name: Anel AG
SRN: CH-MF-000033240
Manufacturer status: Active

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: Mirror plate for resi PRONE
UDI-DI code: 07640372030262
Basic UDI-DI: 764037203PFHT&PFMR83
Reference / catalog number: PFMR
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)

Z12011280PATIENT POSITIONING INSTRUMENTS - 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

Helmet for resi PRONE764037203PFHT&PFMR83On the market resi1764037203resi1ZTOn the market resi PRONE Face Cushion, large764037203PFCJSOn the market resi PRONE Face Cushion, small764037203PFCJSOn the market IMT10764037203imt1AGOn 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.