PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA

FDA Device Registration & Listing · PERSTORP Skane lan [SE-12], SE · Registration 3005139112

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
3005139112
FEI Number
3005139112
Entity Name
PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA
City/State/Country
PERSTORP Skane lan [SE-12], SE
Establishment Address
PERSTORP INDUSTRIAL PARK, PERSTORP Skane lan [SE-12] 284 80, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PERSTORP SPECIALTY CHEMICAL AB (Owner Number: 9010119)
Owner / Operator Contact Address
Perstorp Industrial Park, Perstorp, SE-M 284 80, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K905069
PMA Number
N/A

All Registered Proprietary Names

IODOFLEX IODOSORB GEL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMF Bandage, Liquid General Hospital Class 1 880.5090 2006-03-06
KOZ Beads, Hydrophilic, For Wound Exudate Absorption General, Plastic Surgery Class 1 878.4018 2006-03-06

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

PERSTORP SPECIALTY CHEMICAL 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 3005139112. Last updated year: 2026. Please use registration number 3005139112 when referencing this establishment in official correspondence.
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