Dr. Müller Pharma s.r.o.

CZ-MF-000000005 · Czechia · Hradec Králové

Dr. Müller Pharma s.r.o. is registered in the European database on medical devices as a manufacturer, with 121 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Devices declared under this manufacturer

• ANGINAL® ústní sprej se šalvějí
• Anginal® Spray Buccal á la Sauge
• BILLY BOY Aqua Gleitgel
• ELANEE Befeuchtungs-Gel Classic
• Gel pro sonografii Dr. Müller Pharma
• Müllerovy pastilky® olej čajovníku australského
• Müllerovy pastilky® šalvěj, vitamin C
• Nasumer® Spray Nasal con Dexpantenol
• PURESSENTIEL Respiratoire Comprimés Toux à sucer
• PantheNose® nosní sprej s aloe vera
• PantheNose® ΣΠΡΕΙ ΜΥΤΗΣ ΜΕ ΜΑΓΝΗΣΙΟ
• Pastilky s islandským lišajníkom AKUT

Showing 12 of 121 declared devices.

Catalogue references include PC0203_031, PC2101_001, PC2101_016, PC2109_002, PC4108_003, PC8801_004.

European nomenclature codes declared: V9017, M9002, Q030103, G05, V901001, Z11040185.

United States market access

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

Device-level evidence

Canadian market access

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

North American profile: Neither register. Dr. Müller Pharma s.r.o. was not found in either the U.S. or the Canadian register.

Notified body certificates

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