Identity
- Trade Name
- SPIRETTE® FDA UDI
- Generic Name
- Cervical aspiration catheter FDA UDI
- Device Name
- Device for cervical mucus aspiration FDA UDI
- Model / Reference
- SPIRETTE® FDA UDI
- Description
- Device for cervical mucus aspiration FDA UDI
Identifiers
- Catalog Number
- 1106000 FDA UDI
- Primary DI / UDI-DI
- 03700111400733 FDA UDI
- FDA Product Code
- HDR FDA UDI
- GMDN Term
- Cervical aspiration catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 0.26 Centimeter FDA UDICatheter Length — 26.4 Centimeter FDA UDI
Category: Cervical aspiration catheter
Spirette® by Laboratoire Ccd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cervical aspiration catheter.
- Aspirette — CooperSurgical, Inc. · Class II
- Aspiracath — COOK INCORPORATED · Class II
- MUCAT® STERILE — LABORATOIRE CCD · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Laboratoire Ccd
Sources (1)
- FDA UDI cc633836-3d14-4e89-9d69-6261e3bcbf47 37 fields · synced May 30, 2026