TOUL MEDITECH AB

FDA Device Registration & Listing · Vasteras Vastmanland, SE · Registration 3012992602

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
3012992602
FEI Number
3012992602
Entity Name
TOUL MEDITECH AB
City/State/Country
Vasteras Vastmanland, SE
Establishment Address
Tunbytorpsgatan 31, Vasteras Vastmanland 72137, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Toul Meditech AB (Owner Number: 10052761)
Owner / Operator Contact Address
Tunbytorpsgatan 31, Vasteras, SE-U 72137, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K163455
PMA Number
N/A

All Registered Proprietary Names

SteriStay SurgiCube

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ORC Air Filter Portable Apparatus General, Plastic Surgery Class 2 878.5070 2019-06-20
ORC Air Filter Portable Apparatus General, Plastic Surgery Class 2 878.5070 2024-10-24

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Toul Meditech 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 3012992602. Last updated year: 2026. Please use registration number 3012992602 when referencing this establishment in official correspondence.
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