Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005136445

FEI Number

3005136445

Entity Name

LABORATOIRE CCD

City/State/Country

PARIS Ile-de-France, FR

Establishment Address

36 rue Brunel, PARIS Ile-de-France 75017, FR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

LABORATOIRE CCD (Owner Number: 10061040)

Owner / Operator Contact Address

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

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K983604

PMA Number

N/A

All Registered Proprietary Names

INTRA UTERINE INSEMINATION CANNULA WITH MANDREL MUCAT® STERILE STANDARD INTRA UTERINE INSIMINATION CANNULA SPIRETTE® MEMORY INTRA UTERINE INSEMINATION CANNULA SMALL GENITOR® INTRA UTERINE INSIMINATION CANNULA PIPELLE® PIPELLE® MARK II OPS A.R.T. OF C.C.D. ®WITH VALVE OOCYTE RETRIEVAL NEEDLE 25CM G17 OVO A.R.T. OF C.C.D.® NEEDLE 30CM G17 OOCYTE RETRIEVAL NEEDLE30CM G17 OPS CLASSIC WITH VALVE OPS A.R.T. OF C.C.D. ® WITHOUT VALVE OPS CLASSIC WITHOUT VALVE FULL ECHO®23 CM ECHOGYN ® EMBRYOVIEW M 18 CM CLASSIC ULTRASOFT MOCK 18 CM ULTRASOFT FRYDMAN® SET AVEC WIH GUIDE SHORT FRYDMAN® SET CLASSIC ULTRASOFT MOCK 23 CM FRYDMAN ® SOFT WITH GUIDE ULTRASOFT FRYDMAN ® SET ECHO MOCK CATHETER INVENTCATH ECO ECHOGYN® EMBRYOVIEW M MOCK 23 CM FRYDMAN® CLASSIC 4.5 CLASSIC ULTRASOFT 23 CM ULTRASOFT FRYDMAN® SET MOCK ECHO FULL ECHO® PRO ECHOGYN® EMBRYOVIEW M MOCK 18 CM FRYDMAN® CLASSIC 5.5 ULTRASOFT FRYDMAN ® SET MOCK ECHOGYN®EMBRYOVIEW M 23 CM FRYDMAN® MEMORY STANDARD FRYDMAN® ULTRASOFT T.D.T.®SET STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo CLASSIC ULTRASOFT 18 CM FRYDMAN®ULTRASOFT ECHO ULTRASOFT FRYDMAN ® SET ECHO WITH GUIDE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HDR	Cap, Cervical	Obstetrics/Gynecology	Class 2	884.5250	2019-08-02
HHK	Curette, Suction, Endometrial (And Accessories)	Obstetrics/Gynecology	Class 2	884.1175	2019-08-02
MQE	Needle, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6100	2019-08-02
MQF	Catheter, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6110	2019-08-02

Official Correspondent

Myriam GARCIA

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
K112396	Kitazato Medical Co., Ltd.	IUI CATHETERS	2012-11-02

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1825146	Cook Incorporated	Spencer, IN, US
2246552	Isomedix Operations Inc.	S Plainfield, NJ, US
1216677	COOPERSURGICAL, INC.	Trumbull, CT, US
9612445	PRODIMED	NEUILLY-EN-THELLE Oise, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005136445. Last updated year: 2026. Please use registration number 3005136445 when referencing this establishment in official correspondence.