Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Bone-coring punch, reusable FDA UDI
- Device Name
- KERRISON Bone Punch conventional, 90 °, upwards cutting, 7", (180 mm), width: 2 mm, without ejector, thin, non-sterile, reusable FDA UDI
- Model / Reference
- FF116R FDA UDI
- Description
- KERRISON Bone Punch conventional, 90 °, upwards cutting, 7", (180 mm), width: 2 mm, without ejector, thin, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FF116R FDA UDI
- Primary DI / UDI-DI
- 04046955074754 FDA UDI
- FDA Product Code
- HAE FDA UDI
- GMDN Term
- Bone-coring punch, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4840 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 II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 6e19aa53-b338-4f76-9e39-120a962f9b39 36 fields · synced Jun 1, 2026