Kolplast Ci S A

FDA Filings

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

FDA Registration(s)
Registration Number8044093
FEI Number3005729015
NameKOLPLAST Ci SA
Owner & OperatorKolplast Ci S.A
Contact AddressEstrada Municipal Benedito De Souza #418 Bairro Da Mina
Itupeva BR-SP Sao Paulo 13295-000 BR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressEstrada Municipal Benedito De Souza #418 Bairro Da Mina
Itupeva Sao Paulo, 13295-000 BR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
KOLPLAST Ci SA [Kolplast Ci S.A]
Kolplast Cervical Sample Collection Kit2017-02-14
KOLPLAST CI SA
Kolplast Cervical Sample Collection Kit2017-01-13
KOLPLAST Ci SA [Kolplast Ci S.A]
CellPreserv Preservation Solution2016-11-09
KOLPLAST Ci SA [Kolplast Ci S.A]
CellPreserv Glass Slide2016-11-09
KOLPLAST Ci SA [Kolplast Ci S.A]
CellPreserv Filter2016-11-09
KOLPLAST Ci SA [Kolplast Ci S.A]
Kolplux Vaginal Speculum2014-09-25
KOLPLAST Ci SA [Kolplast Ci S.A]
Kolplux WL System2014-09-25
KOLPLAST Ci SA [Kolplast Ci S.A]
KOLPLUX System2011-09-26
KOLPLAST Ci SA [Kolplast Ci S.A]
Kolplast Vaginal Speculum2007-11-30
KOLPLAST Ci SA [Kolplast Ci S.A]
Kolplast Rectosigmoidoscope1992-06-03

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