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 Number: 3005139112
• FEI Number: 3005139112
• Name: PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA
• Owner & Operator: PERSTORP SPECIALTY CHEMICAL AB
• Contact Address: Perstorp Industrial Park ; 28480 SE-NOTA Perstorp SE
• Official Correspondent:
  • Magnus Fagergren
  • 046-733-133861-x
• US Agent:
  • DAVID LENNARZ
  • Registrar Corp
  • 757 2240177
  • 757 2240179
  • david.lennarz@registrarcorp.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: PERSTORP INDUSTRIAL PARK ; PERSTORP Skane lan [SE-12], 284 80 SE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K940414 | KMF PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]	IODOFLEX	2006-03-06
PMN K905069 | KOZ PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]	IODOSORB GEL	2006-03-06
KOZ PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA [PERSTORP SPECIALTY CHEMICAL AB]	BEADS, HYDROPHILIC	1998-04-07