Identity
- Trade Name
- Aspiracath FDA UDI
- Generic Name
- Cervical aspiration catheter FDA UDI
- Device Name
- Aspiracath FDA UDI
- Model / Reference
- G17270 FDA UDI
- Description
- Aspiracath FDA UDI
Identifiers
- Catalog Number
- J-ASP-092500 FDA UDI
- Primary DI / UDI-DI
- 00827002172708 FDA UDI
- FDA Product Code
- HFC FDA UDI
- GMDN Term
- Cervical aspiration catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1050 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
Yes
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
Category: Cervical aspiration catheter
Aspiracath by Cook Incorporated — 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
- SPIRETTE® — LABORATOIRE CCD · 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
- Cook Incorporated
Sources (1)
- FDA UDI 567166e0-6a8f-4ee7-b3e4-da34e0e78bf0 36 fields · synced Jun 8, 2026