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.
Registration Number | 8044093 |
FEI Number | 3005729015 |
Name | KOLPLAST Ci SA |
Owner & Operator | Kolplast Ci S.A |
Contact Address | Estrada Municipal Benedito De Souza #418 Bairro Da Mina Itupeva BR-SP Sao Paulo 13295-000 BR |
US Agent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | Estrada Municipal Benedito De Souza #418 Bairro Da Mina Itupeva Sao Paulo, 13295-000 BR |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
KOLPLAST Ci SA [Kolplast Ci S.A] | Kolplast Cervical Sample Collection Kit | 2017-02-14 |
KOLPLAST CI SA | Kolplast Cervical Sample Collection Kit | 2017-01-13 |
KOLPLAST Ci SA [Kolplast Ci S.A] | CellPreserv Preservation Solution | 2016-11-09 |
KOLPLAST Ci SA [Kolplast Ci S.A] | CellPreserv Glass Slide | 2016-11-09 |
KOLPLAST Ci SA [Kolplast Ci S.A] | CellPreserv Filter | 2016-11-09 |
KOLPLAST Ci SA [Kolplast Ci S.A] | Kolplux Vaginal Speculum | 2014-09-25 |
KOLPLAST Ci SA [Kolplast Ci S.A] | Kolplux WL System | 2014-09-25 |
KOLPLAST Ci SA [Kolplast Ci S.A] | KOLPLUX System | 2011-09-26 |
KOLPLAST Ci SA [Kolplast Ci S.A] | Kolplast Vaginal Speculum | 2007-11-30 |
KOLPLAST Ci SA [Kolplast Ci S.A] | Kolplast Rectosigmoidoscope | 1992-06-03 |