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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

9001-0XXXX — Class I MDR by EWAC Medical

MD Atlas
EWAC Medical

EUDAMED last updated this device on Aug 21, 2025

9001-0XXXX

87202996139MFBQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EWAC Medical
UDI-DI code: 08720299613904
Reference / catalog number: 9001-0XXXX

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View device family (Basic UDI)

Manufacturer information

Organization name: EWAC Medical
SRN: NL-MF-000013185
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: 08720299613904
Basic UDI-DI: 87202996139MFBQ
Reference / catalog number: 9001-0XXXX
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: With this product the water depth in a pool can be adjusted for optimum use in aquatic therapy. Floor can be set to depths suitable for children, but also for adults. When pool is not in use the floor can be set to water level serving as a thermal and safety cover. Works on water hydraulic, so no contamination of pool water in case of a leakage. The size is pool depending.
Additional information URL: https://www.ewacmedical.com/products/movable-swimming-pool-floor/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720299613904

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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.

Y181899SUPPORT SYSTEMS - OTHER

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.