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Organization name
UDI-DI code
Reference / catalog number

F 5663 — Class I MDR by MEDIPLAST CZ, s.r.o.

MD Atlas
MEDIPLAST CZ, s.r.o.

EUDAMED last updated this device on Mar 27, 2026

F 5663

8595037MEDIPLASTFDZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIPLAST CZ, s.r.o.
UDI-DI code: 08595037956632
Reference / catalog number: F 5663

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Manufacturer information

Organization name: MEDIPLAST CZ, s.r.o.
SRN: CZ-MF-000052351
Manufacturer status: Active

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Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement		Still on market
Slovakia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08595037956632
Basic UDI-DI: 8595037MEDIPLASTFDZ
Reference / catalog number: F 5663
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: Foil plaster with pad 8 cm x 1 m, washable, in box
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M0599MEDICAL PLASTERS - 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.