FDA.reportPublic FDA data

KESSEL MEDINTIM GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30110141783011014178KESSEL MEDINTIM GMBH1N2026-01-01Kelsterbacher Str. 28 Morfelden-Walldorf Hesse DE 64546

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
04013273000116Active Erection System - Vacuum Erection Device for treatment of erectile dysfunction+1301.378.8433kambiz@urologyhealthstore.com
04013273000208Constriction Ring 9mm - Constriction ring or pubic ring to be use together with a vacuump pump for treatment of erectile dysfunction+496105203720export@medintim.de

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1807541288380397K140305CAYA CONTOURED DIAPHRAGMHDW2014-08-26
1807541610117260
1807541758416802
1807541813310172

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HDW12014-08-26

PMN#

GUDID#