Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008727520

FEI Number

3008727520

Entity Name

SCANFIL ATVIDABERG AB

City/State/Country

Atvidaberg Ostergotland, SE

Establishment Address

Orsatter, Atvidaberg Ostergotland 59780, SE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Scanfil Atvidaberg AB (Owner Number: 10034507)

Owner / Operator Contact Address

Orsatter, Atvidaberg, SE-E 59780, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Lucas 3 Lucas 2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRM	Compressor, Cardiac, External	Cardiovascular	Class 2	870.5200	2018-02-14
DRM	Compressor, Cardiac, External	Cardiovascular	Class 2	870.5200	2010-12-07

Official Correspondent

Karin Skullman

US Agent Details

Tynizia Jackman-Davis Email: tynizia.jackman@scanfil.com Phone: (678) 2086940

Related Public Records

Same Entity

Scanfil Atvidaberg 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 3008727520. Last updated year: 2026. Please use registration number 3008727520 when referencing this establishment in official correspondence.