Identity
- Trade Name
- Ct/X Ray Localizer Leksell FDA UDI
- Generic Name
- Head/neck procedure positioner FDA UDI
- Model / Reference
- 41300-3 FDA UDI
Identifiers
- Catalog Number
- 41300-3 FDA UDI
- Primary DI / UDI-DI
- 04056481004040 FDA UDI
- 510(k) Number
- K954861 FDA UDI
- FDA Product Code
- IYE FDA UDI
- GMDN Term
- Head/neck procedure positioner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.5050 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ct/X Ray Localizer Leksell by Brainlab SE — 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
- Brainlab SE
Sources (1)
- FDA UDI 6f17d5e8-d064-4066-b2d4-aa44d76a8c63 36 fields · synced May 30, 2026