CENTROPIX GLOBAL AG

FDA Device Registration & Listing · Ruggell, LI · Registration 3027692296

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
3027692296
FEI Number
3027692296
Entity Name
CENTROPIX GLOBAL AG
City/State/Country
Ruggell, LI
Establishment Address
Industriering 14, Ruggell 9491, LI
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Centropix Global AG (Owner Number: 10089865)
Owner / Operator Contact Address
Industriering 14, Ruggell, LI-06 9491, LI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KLOUD System BUBBLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-01-17

Official Correspondent

Sabrina Gleim

US Agent Details

Anika Gasich Business: Centropix USA, LLC Email: anika@centropix.us Phone: (941) 2533900

Related Public Records

Same Entity

Centropix Global AG
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 3027692296. Last updated year: 2026. Please use registration number 3027692296 when referencing this establishment in official correspondence.
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