Identity
- Trade Name
- Kit, Hand Drill, Cranial FDA UDI
- Generic Name
- Manual surgical rotary handpiece, reusable FDA UDI
- Device Name
- DRILL 24050 VENTRICULOSTOMY CRANIAL FDA UDI
- Model / Reference
- 24050 FDA UDI
- Description
- DRILL 24050 VENTRICULOSTOMY CRANIAL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00643169498457 FDA UDI
- 510(k) Number
- K904283 FDA UDI
- FDA Product Code
- HBG FDA UDI
- GMDN Term
- Manual surgical rotary handpiece, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual surgical rotary handpiece, reusable
Kit, Hand Drill, Cranial by Medtronic PS Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Medtronic PS Medical
Sources (1)
- FDA UDI 68135791-f880-4383-bcb7-33cf0b33545b 35 fields · synced May 30, 2026