FLODINS FILTER AB

FDA Device Registration & Listing · Lysekil Vastra Gotaland, SE · Registration 3007337939

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
3007337939
FEI Number
3007337939
Entity Name
FLODINS FILTER AB
City/State/Country
Lysekil Vastra Gotaland, SE
Establishment Address
Flodins Filter AB, Datavagen 5, Lysekil Vastra Gotaland 45338, SE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Flodins Filter AB (Owner Number: 10044959)
Owner / Operator Contact Address
Flodins Filter AB, Datavagen 5, Lysekil, SE-O 45338, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Servo Guard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAH Filter, Bacterial, Breathing-Circuit Anesthesiology Class 2 868.5260 2013-09-09

Official Correspondent

Anja Thoresson

US Agent Details

Emily Valerio Email: emily.valerio@getinge.com Phone: (862) 2215193

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K962045 Mallinckrodt Medical ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT 1996-11-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007337939. Last updated year: 2026. Please use registration number 3007337939 when referencing this establishment in official correspondence.
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