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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

VSPLK-BLW — Class I MDR by Solutions company

MD Atlas
Solutions company

EUDAMED last updated this device on Feb 1, 2026

VSPLK-BLW

8721249549VSPLK0173

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Solutions company
UDI-DI code: 08721249549694
Reference / catalog number: VSPLK-BLW

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View device family (Basic UDI)

Manufacturer information

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

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SOLCO-OG-M 87215165734OG01W2On the market SOLCO-DH-HND-38 87215165732DH02T6On the market SOLCO-OG-L 87215165734OG01W2On the market SOLCO-DH-VT-30 87215165732DH02T6On the market SOLCO-SSN-BLK-SM8721249549SS019VOn 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

1 warning recorded — scroll inside the panel to see all entries.

CW999
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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: 08721249549694
Basic UDI-DI: 8721249549VSPLK0173
Reference / catalog number: VSPLK-BLW
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 SOLCO Vingerspalk is een herbruikbaar, niet‑steriel medisch hulpmiddel dat is ontworpen om een vinger functioneel te immobiliseren bij lichte letsels. Het hulpmiddel bestaat uit synthetische materialen met een geïntegreerd verstevigend element en een verstelbare klittenbandsluiting.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 8 cm

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08721249549694

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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.

Y060603FINGERS ORTHOSES

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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