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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

N22DAAA1NDIHBXX00111 — Class I MDR by CLINITEX s.r.o.

MD Atlas
CLINITEX s.r.o.

EUDAMED last updated this device on Jan 23, 2026

N22DAAA1NDIHBXX00111

859420696CLIX003SK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLINITEX s.r.o.
UDI-DI code: 08594206967462
Reference / catalog number: N22DAAA1NDIHBXX00111

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Manufacturer information

Organization name: CLINITEX s.r.o.
SRN: CZ-MF-000051598
Manufacturer status: Active

Related devices

N04AAAA1NDIHAXX00108859420696CLIX003SKOn the market N04AAAA1NDIHAXX00008859420696CLIX003SKOn the market N04AAAA1NDIHAXX00908859420696CLIX003SKOn the market N04AAAA1NDIHAXX00109859420696CLIX003SKOn the market N04AAAA1NDIHAXX00009859420696CLIX003SKOn the market

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW999
Nepoužívat aviváž
CW999
Do not use fabric softener
CW010
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: not provided
UDI-DI code: 08594206967462
Basic UDI-DI: 859420696CLIX003SK
Reference / catalog number: N22DAAA1NDIHBXX00111
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: 5XL
Prodloužená
tmavě modrá

EMDN nomenclature code(s)

T0299PROTECTION DRAPES AND GARMENTS - 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

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.