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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

Elastic Tubular Bandage 20m, size… — Class I MDR

MD Atlas
BATIST Medical a.s.

EUDAMED last updated this device on Apr 7, 2026

Elastic Tubular Bandage 20m, size 6, head

8591454doc003M5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BATIST Medical a.s.
UDI-DI code: 08591454006905
Reference / catalog number: 1323300260

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Manufacturer information

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

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: Elastic Tubular Bandage 20m, size 6, head
UDI-DI code: 08591454006905
Basic UDI-DI: 8591454doc003M5
Reference / catalog number: 1323300260
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 20 MU36

EMDN nomenclature code(s)

M03030103TUBULAR NET BANDAGES

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

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