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Sign in to claim this brandLABORATOIRE 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
- —
- —
- [email protected]
- Phone
- +33(0)344266371
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 381633924
Catalogue (49)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Short Frydman® Set | SHORT FRYDMAN® SET | FDA UDI | Class II | Active |
| Full Echo®23 Cm | FULL ECHO®23 CM | FDA UDI | Class II | Active |
| Hoc Collection Vial 30ml | HOC COLLECTION VIAL 30ML | FDA UDI | Class II | Active |
| Ops Classic Without Valve | OPS CLASSIC WITHOUT VALVE | FDA UDI | Class II | Active |
| Echogyn® Embryoview M Mock 23 Cm | ECHOGYN® EMBRYOVIEW M MOCK 23 CM | FDA UDI | Class II | Active |
| Frydman®ultrasoft Echo | FRYDMAN®ULTRASOFT ECHO | FDA UDI | Class II | Active |
| Frydman® Classic 4.5 | FRYDMAN® CLASSIC 4.5 | FDA UDI | Class II | Active |
| Classic Ultrasoft 18 Cm | CLASSIC ULTRASOFT 18 CM | FDA UDI | Class II | Active |
| Inventcath Eco | INVENTCATH ECO | FDA UDI | Class II | Active |
| Classic Ultrasoft 23 Cm | CLASSIC ULTRASOFT 23 CM | FDA UDI | Class II | Active |
| Echogyn® Embryoview M Mock 18 Cm | ECHOGYN® EMBRYOVIEW M MOCK 18 CM | FDA UDI | Class II | Active |
| Ultrasoft Frydman ® Set Mock | ULTRASOFT FRYDMAN ® SET MOCK | FDA UDI | Class II | Active |
| Full Echo® Pro | FULL ECHO® PRO | FDA UDI | Class II | Active |
| Pipelle® | PIPELLE® | FDA UDI | Class II | Active |
| Classic Ultrasoft Mock 23 Cm | CLASSIC ULTRASOFT MOCK 23 CM | FDA UDI | Class II | Active |
| Echogyn ® Embryoview M 18 Cm | ECHOGYN ® EMBRYOVIEW M 18 CM | FDA UDI | Class II | Active |
| Standard Intra Uterine Insimination Cannula | STANDARD INTRA UTERINE INSIMINATION CANNULA | FDA UDI | Class II | Active |
| Hoc2 Classic Without Valve Soft Plug | HOC2 CLASSIC WITHOUT VALVE SOFT PLUG | FDA UDI | Class II | Active |
| Frydman® Memory Standard | FRYDMAN® MEMORY STANDARD | FDA UDI | Class II | Active |
| Ultrasoft Frydman® Set Mock Echo | ULTRASOFT FRYDMAN® SET MOCK ECHO | FDA UDI | Class II | Active |
| Ultrasoft Frydman ® Set Echo With Guide | ULTRASOFT FRYDMAN ® SET ECHO WITH GUIDE | FDA UDI | Class II | Active |
| Mucat® Sterile | MUCAT® STERILE | FDA UDI | Class II | Active |
| 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 II | Active |
| Ops A.r.t. Of C.c.d. ® Without Valve | OPS A.R.T. OF C.C.D. ® WITHOUT VALVE | FDA UDI | Class II | Active |
| Pipelle® Mark Ii | PIPELLE® MARK II | FDA UDI | Class II | Active |
| HOC CLASSIC WITH VALVE Aspiration tube 2 x 33 cm | HOC CLASSIC WITH VALVE Aspiration tube 2 x 33 cm | FDA UDI | Class II | Active |
| Spirette® | SPIRETTE® | FDA UDI | Class II | Active |
| 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 II | Active |
| Small Genitor® Intra Uterine Insimination Cannula | SMALL GENITOR® INTRA UTERINE INSIMINATION CANNULA | FDA UDI | Class II | Active |
| Ops A.r.t. Of C.c.d. ®with Valve | OPS A.R.T. OF C.C.D. ®WITH VALVE | FDA UDI | Class II | Active |
| Echogyn®embryoview M 23 Cm | ECHOGYN®EMBRYOVIEW M 23 CM | FDA UDI | Class II | Active |
| Classic Ultrasoft Mock 18 Cm | CLASSIC ULTRASOFT MOCK 18 CM | FDA UDI | Class II | Active |
| Ops Classic With Valve | OPS CLASSIC WITH VALVE | FDA UDI | Class II | Active |
| Frydman ® Soft With Guide | FRYDMAN ® SOFT WITH GUIDE | FDA UDI | Class II | Active |
| Oocyte Retrieval Needle30cm G17 | OOCYTE RETRIEVAL NEEDLE30CM G17 | FDA UDI | Class II | Active |
| Frydman® Ultrasoft | FRYDMAN® ULTRASOFT | FDA UDI | Class II | Active |
| Hoc A.r.t. Of C.c.d.® Without Valve | HOC A.R.T. OF C.C.D.® WITHOUT VALVE | FDA UDI | Class II | Active |
| Ultrasoft Frydman® Set Avec Wih Guide | ULTRASOFT FRYDMAN® SET AVEC WIH GUIDE | FDA UDI | Class II | Active |
| Mock Catheter | MOCK CATHETER | FDA UDI | Class II | Active |
| Ultrasoft Frydman ® Set Echo | ULTRASOFT FRYDMAN ® SET ECHO | FDA UDI | Class II | Active |
| 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 II | Active |
| Oocyte Retrieval Needle 25cm G17 | OOCYTE RETRIEVAL NEEDLE 25CM G17 | FDA UDI | Class II | Active |
| Frydman® Classic 5.5 | FRYDMAN® CLASSIC 5.5 | FDA UDI | Class II | Active |
| HOC CLASSIC WITHOUT VALVE Aspiration tube 67 cm | HOC CLASSIC WITHOUT VALVE Aspiration tube 67 cm | FDA UDI | Class II | Active |
| Intra Uterine Insemination Cannula With Mandrel | INTRA UTERINE INSEMINATION CANNULA WITH MANDREL | FDA UDI | Class II | Active |
| Hoc A.r.t. Of C.c.d.® With Valve | HOC A.R.T. OF C.C.D.® WITH VALVE | FDA UDI | Class II | Active |
| Memory Intra Uterine Insimination Cannula | MEMORY INTRA UTERINE INSEMINATION CANNULA | FDA UDI | Class II | Active |
| T.d.t.®set | T.D.T.®SET | FDA UDI | Class II | Active |
| STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo | STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Laboratoire Ccd PARIS Ile-de-France · FR FEI 3005136445