Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8030929

FEI Number

1000631051

Entity Name

LJUNGBERG & KOGEL AB

City/State/Country

Helsingborg Skane, SE

Establishment Address

Fågelsångsgatan 10, Helsingborg Skane 25110, SE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ljungberg & Kogel AB (Owner Number: 8030929)

Owner / Operator Contact Address

Fagelsangsgatan 10, Helsingborg, SE-M 25110, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BS CR 6 AA BS CR 4 A BS CR 6 PS AA

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KSD	Device, Heat-Sealing	Hematology	Class 1	864.9750	2013-06-18

Official Correspondent

No official correspondent registered.

US Agent Details

Daniel Kamm Business: Kamm & Associates Email: fda.help.now@gmail.com Phone: (847) 3741727

Related Public Records

Same Entity

Ljungberg & Kogel 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 8030929. Last updated year: 2026. Please use registration number 8030929 when referencing this establishment in official correspondence.