Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9612445

FEI Number

3002807433

Entity Name

PRODIMED

City/State/Country

NEUILLY-EN-THELLE Oise, FR

Establishment Address

4 Avenue De Leurope, NEUILLY-EN-THELLE Oise 60530, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Laboratoire CCD (Owner Number: 9019576)

Owner / Operator Contact Address

36 rue Brunel, --, PARIS, FR-75 75017, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

STANDARD INTRA UTERINE INSIMINATION CANNULA INTRA UTERINE INSEMINATION CANNULA WITH MANDREL MEMORY INTRA UTERINE CANNULA SPIRETTE® MUCAT® STERILE SMALL GENITOR® INTRA UTERINE INSIMINATION CANNULA PIPELLE MARK II PIPELLE Needle Ovo Art of Prodimed OPS ART of Prodimed OVO A.R.T. OF C.C.D.® NEEDLE 30CM G17 OPS A.R.T. OF C.C.D. ® WITHOUT VALVE OPS CLASSIC WITHOUT VALVE OPS A.R.T. OF C.C.D. ®WITH VALVE OPS CLASSIC WITH VALVE OOCYTE RETRIEVAL NEEDLE30CM G17 OOCYTE RETRIEVAL NEEDLE 25CM G17

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HDR	Cap, Cervical	Obstetrics/Gynecology	Class 2	884.5250	2008-03-19
HHK	Curette, Suction, Endometrial (And Accessories)	Obstetrics/Gynecology	Class 2	884.1175	1986-10-29
MQE	Needle, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6100	2008-03-19

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Laboratoire CCD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K082727	Vitrolife Sweden AB	FOLLICLE ASPIRATION SET, REDUCED SINGLE LUMEN	2009-02-06

Similar Registrations

Registration Number	Establishment Name	Location
3013382619	SILCOPLAST AG	Wolfhalden Appenzell Ausserrhoden, CH
1825146	Cook Incorporated	Spencer, IN, US
2246552	Isomedix Operations Inc.	S Plainfield, NJ, US
3005136445	LABORATOIRE CCD	PARIS Ile-de-France, FR
1216677	COOPERSURGICAL, INC.	Trumbull, CT, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9612445. Last updated year: 2026. Please use registration number 9612445 when referencing this establishment in official correspondence.