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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

SOFTPORE Non woven Tape 2,5cmx9,15m — Class I MDR

MD Atlas
BATIST Medical a.s.

EUDAMED last updated this device on Apr 7, 2026

SOFTPORE Non woven Tape 2,5cmx9,15m

8591454doc008MF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BATIST Medical a.s.
UDI-DI code: 08591454003195
Reference / catalog number: 1320103112

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Manufacturer information

Organization name: BATIST Medical a.s.
SRN: CZ-MF-000023038
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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: SOFTPORE Non woven Tape 2,5cmx9,15m
UDI-DI code: 08591454003195
Basic UDI-DI: 8591454doc008MF
Reference / catalog number: 1320103112
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 9.15 MU36
2.5 MU10

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

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Software identification