← Back to catalogue

Procedure pack processed according to Article 22 of the Reg. (EU) 2017/745

EUDAMED

Class I (EU MDR)

Ref 1220130641Model ANGIOGRAFICKÁ ROUŠKA / ANGIOGRAPHY DRAPE

by BATIST Medical Productions s.r.o.

Identity

Trade Name
Procedure pack processed according to Article 22 of the Reg. (EU) 2017/745 EUDAMED
Model / Reference
ANGIOGRAFICKÁ ROUŠKA / ANGIOGRAPHY DRAPE EUDAMED
1220130641 EUDAMED

Identifiers

Primary DI / UDI-DI
08596222866255 EUDAMED
Basic UDI-DI
8596222doc044MT EUDAMED
EMDN Code
M0201010102 COTTON GAUZES, CUT, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Procedure pack processed according to Article 22 of the Reg. (EU) 2017/745 by BATIST Medical Productions s.r.o. — Class I — MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CZ-MF-000023495

Sources (1)

  • EUDAMED 923fe13f-1982-4797-be79-0125f4227f8b 61 fields · synced Jun 18, 2026