Identity
- Trade Name
- Kevor-Curette FDA UDI
- Generic Name
- Endocervical aspirator FDA UDI
- Device Name
- Disposable Endocervical Curette FDA UDI
- Model / Reference
- 66-448B FDA UDI
- Description
- Disposable Endocervical Curette FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937003253 FDA UDI
- 510(k) Number
- K882404 FDA UDI
- FDA Product Code
- PCF FDA UDI
- GMDN Term
- Endocervical aspirator 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
No
FDA UDI
Category: Endocervical aspirator
Kevor-Curette by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endocervical aspirator.
- LUMINELLE Aspirator — Uvision360, Inc. · Class I
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
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 9a8dff28-2c36-4443-b744-18902cf44229 34 fields · synced Jun 9, 2026