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Nosefrida Saline Kit

EUDAMED

Class IIa (EU MDR)

Ref n/a

by Fridababy, LLC

Identity

Device Name
Nosefrida Saline Kit EUDAMED
Model / Reference
n/a EUDAMED

Identifiers

Primary DI / UDI-DI
01220000223455 EUDAMED
Basic UDI-DI
122000022PROJ122ME EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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

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

Category: Device sterilization/disinfection container, reusable

Nosefrida Saline Kit by Fridababy, LLC — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Fridababy, LLC
EUDAMED SRN
US-MF-000044395
Authorised Representative
Nasal Produkter Sverige AB SE-AR-000043090

Sources (1)

  • EUDAMED c1727ef1-322d-49c3-ae05-23bf9107d1d9 61 fields · synced Jun 18, 2026