Identity
- Trade Name
- Centurion FDA UDI
- Generic Name
- General-purpose curette FDA UDI
- Device Name
- STERILE BUCK EAR CURETTE 000 FDA UDI
- Model / Reference
- I86905 FDA UDI
- Description
- STERILE BUCK EAR CURETTE 000 FDA UDI
Identifiers
- Catalog Number
- I86905 FDA UDI
- Primary DI / UDI-DI
- 10653160374862 FDA UDI
- FDA Product Code
- HTF FDA UDI
- GMDN Term
- General-purpose 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
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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose curette
Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose curette.
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
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- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Impulse Interbody Spacer System — Degen Medical · 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
- Centurion Medical Products
Sources (1)
- FDA UDI 9684b2b5-18b3-4217-8ff4-2756df3bc41b 35 fields · synced Jun 7, 2026