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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

1021 — Class I MDR by MEDIPLAST CZ, s.r.o.

MD Atlas
MEDIPLAST CZ, s.r.o.

EUDAMED last updated this device on Mar 23, 2026

1021

8595037MEDIPLASTS7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIPLAST CZ, s.r.o.
UDI-DI code: 08595037910214
Reference / catalog number: 1021

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Manufacturer information

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

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: 08595037910214
Basic UDI-DI: 8595037MEDIPLASTS7
Reference / catalog number: 1021
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 plaster on plastic spool with cover, 2.5 cm x 2 m, with label
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

Related devices

1240 XTK8595037MEDIPLASTtGKOn the market 1220 XTK8595037MEDIPLASTtGKOn the market 1230 XTK8595037MEDIPLASTtGKOn the market 12308595037MEDIPLASTtGKOn the market 12408595037MEDIPLASTtGKOn 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.