Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- General-purpose curette FDA UDI
- Device Name
- Ring Curette, 90 °, angled, 10 1/2", (265 mm), sharp, width: 3 mm, non-sterile, reusable FDA UDI
- Model / Reference
- MF126R FDA UDI
- Description
- Ring Curette, 90 °, angled, 10 1/2", (265 mm), sharp, width: 3 mm, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- MF126R FDA UDI
- Primary DI / UDI-DI
- 04046964979958 FDA UDI
- FDA Product Code
- KAP FDA UDI
- GMDN Term
- General-purpose curette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Aesculap, Inc.
Sources (1)
- FDA UDI b94ca810-4671-45de-9504-e91d568fb53b 36 fields · synced May 31, 2026