Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Craniofacial rongeur, reusable FDA UDI
- Device Name
- KERRISON Bone Punch conventional, 90 °, upwards cutting, 7", (180 mm), regular, width: 6 mm, opening width: 12 mm, detachable, withejector, standard, non-sterile, reusable FDA UDI
- Model / Reference
- FK953R FDA UDI
- Description
- KERRISON Bone Punch conventional, 90 °, upwards cutting, 7", (180 mm), regular, width: 6 mm, opening width: 12 mm, detachable, withejector, standard, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FK953R FDA UDI
- Primary DI / UDI-DI
- 04038653300068 FDA UDI
- FDA Product Code
- LRY FDA UDI
- GMDN Term
- Craniofacial rongeur, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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 1f2ae770-c9c5-43a6-a790-ac3102a0f4d0 36 fields · synced May 31, 2026