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BATIST Medical Productions s.r.o.

CZ-MF-000023495 · Czechia · Červený Kostelec

BATIST Medical Productions s.r.o. is registered in the European database on medical devices as a manufacturer, with 354 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa354

Most frequent device types declared: ANGIOGRAFICKÁ ROUŠKA / ANGIOGRAPHY DRAPE.

Among these devices, 42 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 354 declared devices.

Catalogue references include 1220692307B, 1220698137, 1220698204, 1230100562, 1230100607T, 1230118102.

European nomenclature codes declared: T020102, M040404, M0201020102, M030101, T030199, M020199.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED354
Country of registrationCzechia

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN354
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. BATIST Medical Productions s.r.o. was not found in either the U.S. or the Canadian register.

Notified body certificates

CertificateStatusExpiry
24 0234 QR/NBsupplemented2029-06-25

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