Konsultbyran Process Construction AB

FDA Device Registration & Listing · Tommarp Skane, SE · Registration 3009143236

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
3009143236
FEI Number
3009143236
Entity Name
Konsultbyran Process Construction AB
City/State/Country
Tommarp Skane, SE
Establishment Address
Tagarpsvagen 2, Tommarp Skane 27293, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Konsultbyran Process Construction AB (Owner Number: 10040190)
Owner / Operator Contact Address
Tagarpsvagen 2, Tommarp, SE-NOTA 27293, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LWK Razor, Surgical General, Plastic Surgery Class 1 878.4800 2012-03-16

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

Konsultbyran Process Construction AB
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009143236. Last updated year: 2026. Please use registration number 3009143236 when referencing this establishment in official correspondence.
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