Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Dental spatula, reusable FDA UDI
- Device Name
- PLASTIC FILLING INSTRUMENT CONTRA ANGLE FDA UDI
- Model / Reference
- DE101R FDA UDI
- Description
- PLASTIC FILLING INSTRUMENT CONTRA ANGLE FDA UDI
Identifiers
- Catalog Number
- DE101R FDA UDI
- Primary DI / UDI-DI
- 04038653034253 FDA UDI
- FDA Product Code
- EIY FDA UDI
- GMDN Term
- Dental spatula, reusable 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
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 d66a4cbc-fccc-41ec-b0e8-5bf4164cb00f 36 fields · synced Jun 1, 2026