Identity
- Trade Name
- Leksell Vantage Stereotactic System FDA UDI
- Generic Name
- Neurological stereotactic surgery system FDA UDI
- Device Name
- MRI COIL ADAPTER UNIVERSAL FDA UDI
- Model / Reference
- 1053930 FDA UDI
- Description
- MRI COIL ADAPTER UNIVERSAL FDA UDI
Identifiers
- Catalog Number
- 1053930 FDA UDI
- Primary DI / UDI-DI
- 07340048304351 FDA UDI
- 510(k) Number
- K171123 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Neurological stereotactic surgery system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Neurological stereotactic surgery system
Leksell Vantage Stereotactic System by Elekta Instrument AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K171123 also covers:
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
- Leksell Vantage Stereotactic System — Elekta Instrument AB
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
- Elekta Instrument AB
Sources (1)
- FDA UDI e3282088-fd9c-4f68-9abd-593d8e903d1c 36 fields · synced Jun 1, 2026