Identity
- Trade Name
- Kevorkian Curette FDA UDI
- Generic Name
- Endometrial biopsy curette FDA UDI
- Device Name
- Kevorkian Curette with basket FDA UDI
- Model / Reference
- 66-442 FDA UDI
- Description
- Kevorkian Curette with basket FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937017373 FDA UDI
- FDA Product Code
- FZS FDA UDI
- GMDN Term
- Endometrial biopsy curette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 305 Millimeter FDA UDI
Category: Endometrial biopsy curette
Kevorkian Curette by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endometrial biopsy curette.
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- Gimmi — Gimmi GmbH · Class I
- Gimmi — Gimmi GmbH · Class I
- Gynex — GYNEX CORPORATION · Class I
- PILLING — TELEFLEX INCORPORATED · 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 I | Pending data |
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Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 776bd6ec-a4bf-4f95-ab09-3f5ef94b4cd1 34 fields · synced Jun 9, 2026