Identity
- Trade Name
- Surgical Direct FDA UDI
- Generic Name
- Ear excavator FDA UDI
- Device Name
- 6 1/2" Buck Ear Curette Blunt, Size 000, Straight FDA UDI
- Model / Reference
- SD92053304 FDA UDI
- Description
- 6 1/2" Buck Ear Curette Blunt, Size 000, Straight FDA UDI
Identifiers
- Catalog Number
- SD92053304 FDA UDI
- Primary DI / UDI-DI
- B382SD920533040 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Ear excavator 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
No
FDA UDI
Prescription Use
No
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
Category: Ear excavator
Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- V. Mueller — STERIS CORPORATION · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · 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
- Surgical Direct, Inc.
Sources (1)
- FDA UDI 6416b0da-635d-4dd0-bb6c-29e1eaca2d37 35 fields · synced May 30, 2026