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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

1532.04 — Class I MDR by Viacell s.r.o.

MD Atlas
Viacell s.r.o.

EUDAMED last updated this device on May 27, 2026

1532.04

85940621400TD001W6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Viacell s.r.o.
UDI-DI code: 08594062142164
Reference / catalog number: 1532.04

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View device family (Basic UDI)

Manufacturer information

Organization name: Viacell s.r.o.
SRN: CZ-MF-000051827
Manufacturer status: Active

Related devices

1986.0485940621400TD001W6On the market 1101.04 85940621400TD001W6On the market 1209.0485940621400TD001W6On the market 1016.0485940621400TD001W6On the market 1014.04 85940621400TD001W6On 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement	Jun 5, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594062142164
Basic UDI-DI: 85940621400TD001W6
Reference / catalog number: 1532.04
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: 20
Additional product description: Náplasti určené k ošetření odřenin a drobných poranění
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M04010199ADHESIVE DRESSINGS, WITH ABSORBENT PAD - 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

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