Perstorp Specialty Chemical Ab

FDA Filings

This page includes the latest FDA filings for Perstorp Specialty Chemical Ab. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005139112
FEI Number3005139112
NamePERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA
Owner & OperatorPERSTORP SPECIALTY CHEMICAL AB
Contact AddressPerstorp Industrial Park
28480 SE-NOTA Perstorp SE
Official Correspondent
  • Magnus Fagergren
  • 046-733-133861-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressPERSTORP INDUSTRIAL PARK
PERSTORP Skane lan [SE-12], 284 80 SE
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]
IODOFLEX2006-03-06
PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]
IODOSORB GEL2006-03-06
PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]
BEADS, HYDROPHILIC1998-04-07

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