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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

SOLCO-DH-HND-38 — Class I MDR by Solutions company

MD Atlas
Solutions company

EUDAMED last updated this device on May 22, 2026

SOLCO-DH-HND-38

87215165732DH02T6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Solutions company
UDI-DI code: 08721516573292
Reference / catalog number: SOLCO-DH-HND-38

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View device family (Basic UDI)

Manufacturer information

Organization name: Solutions company
SRN: NL-MF-000051126
Manufacturer status: Active

Related devices

SOLCO-OG-M 87215165734OG01W2On the market SOLCO-OG-L 87215165734OG01W2On the market SOLCO-DH-VT-30 87215165732DH02T6On the market SOLCO-SSN-BLK-SM8721249549SS019VOn the market SOLCO-DH-LEG-65 87215165732DH02T6On 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Jun 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08721516573292
Basic UDI-DI: 87215165732DH02T6
Reference / catalog number: SOLCO-DH-HND-38
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: SOLCO Douchehoes / Gipshoes – herbruikbare waterdichte beschermhoes (per stuk) met een transparante waterdichte sleeve (TPU) en een huidvriendelijke, latexvrije siliconen seal. De hoes wordt over arm of been aangebracht om gips, verband, wondbedekking of huid te beschermen tegen water tijdens douchen of kortdurend wassen. De been anti-slip variant bevat een geïntegreerde anti-slip zool/structuur voor extra grip op natte oppervlakken.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 38cm

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08721516573292

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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.

Y093399WASHING, BATHING AND SHOWERING DEVICES - 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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