AIRSONETT AB

FDA Device Registration & Listing · Angelholm Skane, SE · Registration 3004793042

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004793042
FEI Number
3004793042
Entity Name
AIRSONETT AB
City/State/Country
Angelholm Skane, SE
Establishment Address
Kelliehousevagen 31, Angelholm Skane 26274, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Airsonett AB (Owner Number: 10027949)
Owner / Operator Contact Address
Kelliehousevagen 31, Angelholm, SE-M 26274, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K130702
PMA Number
N/A

All Registered Proprietary Names

Airsonett

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRF Cleaner, Air, Medical Recirculating General Hospital Class 2 880.5045 2013-12-17

Official Correspondent

No official correspondent registered.

US Agent Details

Cherita James Business: Pro Pharma Group Email: cherita.james@propharmagroup.com Phone: (347) 9540624

Related Public Records

Same Entity

Airsonett AB
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004793042. Last updated year: 2026. Please use registration number 3004793042 when referencing this establishment in official correspondence.
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