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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

ERGOtip 5 (M) — Class I MDR by Danrehab A/S

MD Atlas
Danrehab A/S

EUDAMED last updated this device on May 29, 2026

ERGOtip 5 (M)

571506409120323EL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Danrehab A/S
UDI-DI code: 05745000463411
Reference / catalog number: 35321

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View device family (Basic UDI)

Manufacturer information

Organization name: Danrehab A/S
SRN: DK-MF-000024162
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement		Still on market

Device identification

Trade name: ERGOtip 5 (M)
UDI-DI code: 05745000463411
Basic UDI-DI: 571506409120323EL
Reference / catalog number: 35321
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: Bath- and toilet chair
Additional information URL: https://danrehab.dk/ergotip-5-m
Clinical sizes: 25–150 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05745000463411

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y093303FIXED AND ROTARY CHAIRS FOR BATH AND SHOWER

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

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Related devices

BUZZ 1571506409120324ENOn the market ERGOtip 10 (M)571506409120323ELOn the market ERGOtip 11 (XXL)571506409120323ELOn the market 108829571506409120323ELOn the market ERGOtip 5 (M) Anytoilet571506409120323ELOn 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.