Identity
- Trade Name
- American Eagle Instruments FDA UDI
- Generic Name
- Dental rongeur FDA UDI
- Device Name
- FORCEPS AMERICAN A 23 FDA UDI
- Model / Reference
- AEFA1167 FDA UDI
- Description
- FORCEPS AMERICAN A 23 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841013105470 FDA UDI
- FDA Product Code
- JEX FDA UDI
- GMDN Term
- Dental rongeur FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
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
Dry Heat Sterilization FDA UDI
American Eagle Instruments by American Eagle Instruments — 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
- American Eagle Instruments
Sources (1)
- FDA UDI cd4fc9ac-cc1e-4a64-a8af-2074f4ec6e0a 34 fields · synced Jun 9, 2026