Paul Hartmann S A

FDA Filings

This page includes the latest FDA filings for Paul Hartmann S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Paul Hartmann S A holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3009080375
FEI Number3009080375
NamePAUL HARTMANN S.A.
Owner & OperatorPAUL HARTMANN AG
Contact Address481 Lakeshore Parkway --
Rock Hill SC 29730 US
Official Correspondent
  • Diane Marsilio
  • 001-803-9851120-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressP.I. Pla d en Boet II Carrasco i Formiguera, 48
Matar? Barcelona, E-08302 ES
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
PAUL HARTMANN S.A. [PAUL HARTMANN AG]
FLEX-BAND AND OMNIFIX2006-11-15
PAUL HARTMANN S.A. [PAUL HARTMANN AG]
COSMOPORE2006-11-15

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