SONESTA MEDICAL AB

FDA Device Registration & Listing · Stockholm, SE · Registration 3010496070

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
3010496070
FEI Number
3010496070
Entity Name
SONESTA MEDICAL AB
City/State/Country
Stockholm, SE
Establishment Address
Industrivagen 7, 171 48 Solna, Stockholm 114 46, SE
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Sonesta Medical AB (Owner Number: 10047317)
Owner / Operator Contact Address
Industrivagen 7,, Solna, SE-AB 171 48, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMZ Table, Cystometric, Electric Gastroenterology, Urology Class 2 876.4890 2014-08-07

Official Correspondent

No official correspondent registered.

US Agent Details

Elisa Maldonaldo-Holmertz Business: Obelix consulting LLC Email: elisamh@obelixconsult.com Phone: (512) 4316069

Related Public Records

Same Entity

Sonesta Medical 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 3010496070. Last updated year: 2026. Please use registration number 3010496070 when referencing this establishment in official correspondence.
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