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Tetesept Bronchosan Spray

EUDAMED

Class IIa (EU MDR)

Ref 20002117

by PK Benelux BV

Identity

Trade Name
Tetesept Bronchosan Spray EUDAMED
Device Name
Bronchosan Spray EUDAMED
Model / Reference
20002117 EUDAMED

Identifiers

Primary DI / UDI-DI
D-200021173Q EUDAMED
Basic UDI-DI
B-200021173Q EUDAMED
EMDN Code
R028099 RESPIRATORY CIRCUITS AND MOUNT CATHETERS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Tetesept Bronchosan Spray by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (1)

  • EUDAMED 9a2ea404-c253-4c85-8f70-37edda9fa8b9 61 fields · synced Jul 9, 2026