YOURRAD AB

FDA Device Registration & Listing · Kungsbacka Halland, SE · Registration 3020847627

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
3020847627
FEI Number
3020847627
Entity Name
YOURRAD AB
City/State/Country
Kungsbacka Halland, SE
Establishment Address
Tryckarevagen 7, Kungsbacka Halland 43447, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
YourRad AB (Owner Number: 10087462)
Owner / Operator Contact Address
Tryckarevagen 7, Kungsbacka, SE-NOTA 43447, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Medena Ilieostomy catheter straight 30 fr Medena Urostomy catheter straight 24 fr

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPH Catheter, Rectal For Continent Ileostomy Gastroenterology, Urology Class 1 876.5030 2023-03-02

Official Correspondent

No official correspondent registered.

US Agent Details

Emily Matorin Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

YourRad 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 3020847627. Last updated year: 2026. Please use registration number 3020847627 when referencing this establishment in official correspondence.
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