Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- General-purpose surgical spatula FDA UDI
- Device Name
- SLOANE LASEK EPI PEELER 115MM FDA UDI
- Model / Reference
- MA781R FDA UDI
- Description
- SLOANE LASEK EPI PEELER 115MM FDA UDI
Identifiers
- Catalog Number
- MA781R FDA UDI
- Primary DI / UDI-DI
- 04046964675454 FDA UDI
- FDA Product Code
- HND FDA UDI
- GMDN Term
- General-purpose surgical spatula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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 02b0df12-d04a-4f22-ac90-a7bf7f6c98a7 36 fields · synced May 31, 2026