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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

220 692 — Class I MDR by MEDI help

MD Atlas
MEDI help

EUDAMED last updated this device on Apr 21, 2026

220 692

426041834BedMHB8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDI help
UDI-DI code: 04260418340235
Reference / catalog number: 220 692

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Manufacturer information

Organization name: MEDI help
SRN: DE-MF-000006421
Manufacturer status: Active

Related devices

275 693426041834BedMHB8On the market 275 691426041834BedMHB8On the market 275 692426041834BedMHB8On the market 220 693426041834BedMHB8On the market 220 691426041834BedMHB8On 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.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260418340235
Basic UDI-DI: 426041834BedMHB8
Reference / catalog number: 220 692
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: Hospitales Krankenbett MEDI help, 3-geteilte Liegefläche, 900 mm
Additional information URL: https://www.medi-help.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080602MANUAL MEDICAL BEDS

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