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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

Spycra Sil-Tape — Class I MDR by Reskin Medical NV

MD Atlas
Reskin Medical NV

EUDAMED last updated this device on Oct 2, 2025

Spycra Sil-Tape

5430002895SPYSIL9P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Reskin Medical NV
UDI-DI code: 05430002895024
Reference / catalog number: SPYSIL-253000

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Manufacturer information

Organization name: Reskin Medical NV
SRN: BE-MF-000012226
Manufacturer status: Active

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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.

Market distribution

Primary placement in Denmark; available across 1 country total.

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

Device identification

Trade name: Spycra Sil-Tape
UDI-DI code: 05430002895024
Basic UDI-DI: 5430002895SPYSIL9P
Reference / catalog number: SPYSIL-253000
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: 12
Additional product description: Spycra Sil-Tape is soft, non-irritating and is easy to apply and remove, the silicone gel layer assures fixation and gentle removal. lt is designed for fixation of medical devices such as drains, tubes, probes, electrodes and so on, and can offer gentle skin protection.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

H900299TAPES, MEDICAL/SURGICAL - 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

UDI-PI traceability

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Manufacturing date
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Software identification