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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

Pakpaak met beugel 80 cm — Class I MDR by Aleidis Specials B.V.

MD Atlas
Aleidis Specials B.V.

EUDAMED last updated this device on Nov 5, 2024

Pakpaak met beugel 80 cm

87208924328278H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aleidis Specials B.V.
UDI-DI code: 08720892432827
Reference / catalog number: Pakpaak met beugel 80 cm

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Manufacturer information

Organization name: Aleidis Specials B.V.
SRN: NL-MF-000044684
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08720892432827
Basic UDI-DI: 87208924328278H
Reference / catalog number: Pakpaak met beugel 80 cm
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: De Pakpaal is een hulpmiddel wat flexibel in te zetten in een woning bedoeld voor alle mensen die beperkt zijn in hun bewegingsapparaat en hulp nodig hebben bij gaan zitten, opstaan of omdraaien in bed. De Pakpaal kan op elke willekeurige plek in een woning conform de voorwaarden uit deze handleiding gemonteerd worden. Dit type Pakpaal is niet geschikt voor natte ruimtes.
Additional information URL: https://pakpaal.nl/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Y050202STANDING FRAMES

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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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.