FDA Device Registration & Listing · Morfelden-Walldorf Hesse, DE · Registration 3011014178
Public RecordDevice ListingExpiry Year: 2026
This page presents structured fields from public FDA datasets.
Registration Header Parameters
Normalized identity and public registration information from FDA records.
Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011014178
FEI Number
3011014178
Entity Name
KESSEL MEDINTIM GMBH
City/State/Country
Morfelden-Walldorf Hesse,
DE
Establishment Address
Kelsterbacher Str. 28, Morfelden-Walldorf Hesse 64546, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kessel medintim GmbH (Owner Number: 10048803)
Owner / Operator Contact Address
Kelsterbacher Str. 28, Morfelden-Walldorf, DE-HE 64546, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A
All Registered Proprietary Names
Vagiwell Dilators Set LargeVagiwell Dilators Set SmallVagiwell Dilators Set PremiumProsecca BandCaya contoured diaphragmRehabi Penile Vacuum TrainerManual Erection SystemActive3 Erection SystemConstriction ring 9mmConstriction ring 12 mmConstriction ring 18mmConstriction ring 21mmConstriction ring 15mm
Source Citation & Summary:
This public preview is extracted from openFDA device registration and listing logs under registration number 3011014178.
Last updated year: 2026.
Please use registration number 3011014178 when referencing this establishment in official correspondence.
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