Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

LABORATOIRE CCD

US

Last updated May 24, 2026

What LABORATOIRE CCD makes

The company manufactures single-use medical devices for assisted reproduction and cervical diagnostics, including transfer catheters (such as the Frydman® Classic and Ultrasoft variants), oocyte aspiration needles, cervical aspiration catheters, cytology brushes, and cryotubes for embryo storage. Devices like the SHORT FRYDMAN® SET and FULL ECHO® 23 CM are designed for embryo transfer procedures, while the HOC Collection Vial 30ML and OPS Classic (without valve) serve embryo or oocyte handling. Cervical sampling tools, such as the ECHOGYN® EmbryoView M mock catheters, are also part of the portfolio, alongside mock training devices for procedural practice.

These devices fall under FDA Class II regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within US regulatory frameworks, ensuring compliance with applicable medical device standards for reproductive and diagnostic applications.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Laboratoire CCD manufacture?

Laboratoire CCD specializes in single-use medical devices primarily for assisted reproduction and cervical diagnostics. Their portfolio includes transfer catheters (such as Frydman® Classic and Ultrasoft variants), oocyte aspiration needles, cervical aspiration catheters, cervical cytology brushes, and cryotubes for embryo storage. These devices are designed for procedures like embryo transfer, oocyte retrieval, and cervical sampling, ensuring compatibility with reproductive health applications.

Where is Laboratoire CCD based, and how does this affect its regulatory compliance?

Laboratoire CCD is based in the US, which means its devices must comply with FDA regulations. Since these devices fall under FDA Class II classification, they are subject to stricter controls compared to Class I devices, including mandatory registration, listing, and adherence to performance standards. The company’s devices are also listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and regulatory transparency.

Which regulatory registries or databases list Laboratoire CCD’s devices?

Laboratoire CCD’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution lifecycle, ensuring regulatory oversight and patient safety. This listing is required for Class II devices under FDA regulations, providing transparency for healthcare providers and regulators.

How are Laboratoire CCD’s devices classified by regulatory authorities?

Laboratoire CCD’s devices are classified as FDA Class II under US regulations. This classification indicates a moderate risk level, requiring compliance with specific controls such as design reviews, manufacturing process validation, and post-market surveillance. Class II devices are subject to stricter regulatory scrutiny than Class I but not as stringent as Class III, which are typically higher-risk devices.

What are some examples of devices manufactured by Laboratoire CCD, and what are they used for?

Laboratoire CCD manufactures devices like the SHORT FRYDMAN® SET (used for embryo transfer) and FULL ECHO® 23 CM (another transfer catheter variant), which are essential for assisted reproduction procedures. The HOC Collection Vial 30ML and OPS Classic (without valve) are designed for handling embryos or oocytes, while cervical sampling tools like the ECHOGYN® EmbryoView M mock catheters assist in diagnostic procedures. Mock training devices, such as the ULTRASOFT FRYDMAN® SET MOCK, are also part of their portfolio for procedural practice.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
ccdlab.com
LinkedIn
—
Facebook
—
Phone
+33(0)344266371
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
381633924

Catalogue (49)

DeviceModel / ReferenceRegistriesClassStatus
Short Frydman® Set SHORT FRYDMAN® SET
FDA UDI
Class IIActive
Full Echo®23 Cm FULL ECHO®23 CM
FDA UDI
Class IIActive
Hoc Collection Vial 30ml HOC COLLECTION VIAL 30ML
FDA UDI
Class IIActive
Ops Classic Without Valve OPS CLASSIC WITHOUT VALVE
FDA UDI
Class IIActive
Echogyn® Embryoview M Mock 23 Cm ECHOGYN® EMBRYOVIEW M MOCK 23 CM
FDA UDI
Class IIActive
Frydman®ultrasoft Echo FRYDMAN®ULTRASOFT ECHO
FDA UDI
Class IIActive
Frydman® Classic 4.5 FRYDMAN® CLASSIC 4.5
FDA UDI
Class IIActive
Classic Ultrasoft 18 Cm CLASSIC ULTRASOFT 18 CM
FDA UDI
Class IIActive
Inventcath Eco INVENTCATH ECO
FDA UDI
Class IIActive
Classic Ultrasoft 23 Cm CLASSIC ULTRASOFT 23 CM
FDA UDI
Class IIActive
Echogyn® Embryoview M Mock 18 Cm ECHOGYN® EMBRYOVIEW M MOCK 18 CM
FDA UDI
Class IIActive
Ultrasoft Frydman ® Set Mock ULTRASOFT FRYDMAN ® SET MOCK
FDA UDI
Class IIActive
Full Echo® Pro FULL ECHO® PRO
FDA UDI
Class IIActive
Pipelle® PIPELLE®
FDA UDI
Class IIActive
Classic Ultrasoft Mock 23 Cm CLASSIC ULTRASOFT MOCK 23 CM
FDA UDI
Class IIActive
Echogyn ® Embryoview M 18 Cm ECHOGYN ® EMBRYOVIEW M 18 CM
FDA UDI
Class IIActive
Standard Intra Uterine Insimination Cannula STANDARD INTRA UTERINE INSIMINATION CANNULA
FDA UDI
Class IIActive
Hoc2 Classic Without Valve Soft Plug HOC2 CLASSIC WITHOUT VALVE SOFT PLUG
FDA UDI
Class IIActive
Frydman® Memory Standard FRYDMAN® MEMORY STANDARD
FDA UDI
Class IIActive
Ultrasoft Frydman® Set Mock Echo ULTRASOFT FRYDMAN® SET MOCK ECHO
FDA UDI
Class IIActive
Ultrasoft Frydman ® Set Echo With Guide ULTRASOFT FRYDMAN ® SET ECHO WITH GUIDE
FDA UDI
Class IIActive
Mucat® Sterile MUCAT® STERILE
FDA UDI
Class IIActive
Hoc2 A.r.t. Of C.c.d. ®with Valve Soft Plug HOC2 A.R.T. OF C.C.D. ®WITH VALVE SOFT PLUG
FDA UDI
Class IIActive
Ops A.r.t. Of C.c.d. ® Without Valve OPS A.R.T. OF C.C.D. ® WITHOUT VALVE
FDA UDI
Class IIActive
Pipelle® Mark Ii PIPELLE® MARK II
FDA UDI
Class IIActive
HOC CLASSIC WITH VALVE Aspiration tube 2 x 33 cm HOC CLASSIC WITH VALVE Aspiration tube 2 x 33 cm
FDA UDI
Class IIActive
Spirette® SPIRETTE®
FDA UDI
Class IIActive
Ovo A.r.t. Of C.c.d.® Needle 30cm G17 OVO A.R.T. OF C.C.D.® NEEDLE 30CM G17
FDA UDI
Class IIActive
Small Genitor® Intra Uterine Insimination Cannula SMALL GENITOR® INTRA UTERINE INSIMINATION CANNULA
FDA UDI
Class IIActive
Ops A.r.t. Of C.c.d. ®with Valve OPS A.R.T. OF C.C.D. ®WITH VALVE
FDA UDI
Class IIActive
Echogyn®embryoview M 23 Cm ECHOGYN®EMBRYOVIEW M 23 CM
FDA UDI
Class IIActive
Classic Ultrasoft Mock 18 Cm CLASSIC ULTRASOFT MOCK 18 CM
FDA UDI
Class IIActive
Ops Classic With Valve OPS CLASSIC WITH VALVE
FDA UDI
Class IIActive
Frydman ® Soft With Guide FRYDMAN ® SOFT WITH GUIDE
FDA UDI
Class IIActive
Oocyte Retrieval Needle30cm G17 OOCYTE RETRIEVAL NEEDLE30CM G17
FDA UDI
Class IIActive
Frydman® Ultrasoft FRYDMAN® ULTRASOFT
FDA UDI
Class IIActive
Hoc A.r.t. Of C.c.d.® Without Valve HOC A.R.T. OF C.C.D.® WITHOUT VALVE
FDA UDI
Class IIActive
Ultrasoft Frydman® Set Avec Wih Guide ULTRASOFT FRYDMAN® SET AVEC WIH GUIDE
FDA UDI
Class IIActive
Mock Catheter MOCK CATHETER
FDA UDI
Class IIActive
Ultrasoft Frydman ® Set Echo ULTRASOFT FRYDMAN ® SET ECHO
FDA UDI
Class IIActive
Hoc2 A.r.t. Of C.c.d.® Without Valve Soft Plug HOC2 A.R.T. OF C.C.D.® WITHOUT VALVE SOFT PLUG
FDA UDI
Class IIActive
Oocyte Retrieval Needle 25cm G17 OOCYTE RETRIEVAL NEEDLE 25CM G17
FDA UDI
Class IIActive
Frydman® Classic 5.5 FRYDMAN® CLASSIC 5.5
FDA UDI
Class IIActive
HOC CLASSIC WITHOUT VALVE Aspiration tube 67 cm HOC CLASSIC WITHOUT VALVE Aspiration tube 67 cm
FDA UDI
Class IIActive
Intra Uterine Insemination Cannula With Mandrel INTRA UTERINE INSEMINATION CANNULA WITH MANDREL
FDA UDI
Class IIActive
Hoc A.r.t. Of C.c.d.® With Valve HOC A.R.T. OF C.C.D.® WITH VALVE
FDA UDI
Class IIActive
Memory Intra Uterine Insimination Cannula MEMORY INTRA UTERINE INSEMINATION CANNULA
FDA UDI
Class IIActive
T.d.t.®set T.D.T.®SET
FDA UDI
Class IIActive
STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Laboratoire Ccd PARIS Ile-de-France · FR FEI 3005136445