Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Q30DAAA1KDUHAXX00XXX — Class I MDR by CLINITEX s.r.o.

MD Atlas
CLINITEX s.r.o.

EUDAMED last updated this device on Jan 23, 2026

Q30DAAA1KDUHAXX00XXX

859420696CLIX005SP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLINITEX s.r.o.
UDI-DI code: 08594206968162
Reference / catalog number: Q30DAAA1KDUHAXX00XXX

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

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: 08594206968162
Basic UDI-DI: 859420696CLIX005SP
Reference / catalog number: Q30DAAA1KDUHAXX00XXX
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: 60 MU10
60 MU10
světle modrá

EMDN nomenclature code(s)

T020199SURGICAL DRAPES - 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

N04AAAA1NDIHAXX00108859420696CLIX003SKOn the market N04AAAA1NDIHAXX00008859420696CLIX003SKOn the market N04AAAA1NDIHAXX00908859420696CLIX003SKOn the market N04AAAA1NDIHAXX00109859420696CLIX003SKOn the market N04AAAA1NDIHAXX00009859420696CLIX003SK

On the market