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Organization name
UDI-DI code
Reference / catalog number

1230 XTK — Class I MDR by MEDIPLAST CZ, s.r.o.

MD Atlas
MEDIPLAST CZ, s.r.o.

EUDAMED last updated this device on Apr 20, 2026

1230 XTK

8595037MEDIPLASTtGK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIPLAST CZ, s.r.o.
UDI-DI code: 08595037912317
Reference / catalog number: 1230 XTK

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Manufacturer information

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

Related devices

1240 XTK8595037MEDIPLASTtGKOn the market 1220 XTK8595037MEDIPLASTtGKOn the market 12308595037MEDIPLASTtGKOn the market 12408595037MEDIPLASTtGKOn the market 12108595037MEDIPLASTtGKOn 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.

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: 08595037912317
Basic UDI-DI: 8595037MEDIPLASTtGK
Reference / catalog number: 1230 XTK
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: Textile tape plaster 3.8 cm x 10 m in a 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)

M030403FUNCTIONAL BANDAGES WITH ANELASTIC TAPES

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
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Software identification