Identity
- Trade Name
- SmartAblateTM System Remote Control FDA UDI
- Generic Name
- Percutaneous radio-frequency ablation system generator FDA UDI
- Model / Reference
- M490009 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260166371437 FDA UDI
- FDA Product Code
- LPB FDA UDI
- GMDN Term
- Percutaneous radio-frequency ablation system generator FDA UDI
Classification
- Device Class
- Class III 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
Yes
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
Category: Percutaneous radio-frequency ablation system generator
SmartAblateTM System Remote Control by Stockert GmbH — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Percutaneous radio-frequency ablation system generator.
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- Maestro 4000™ Controller — Boston Scientific · Class III
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- Electrosurgical Pencil, Button Switch — DEROYAL INDUSTRIES, INC. · Class IIb
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
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 III | Pending data |
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Manufacturer
- Manufacturer
- Stockert GmbH
Sources (1)
- FDA UDI b36e882c-bb69-4933-8f6c-7e73d62fce45 32 fields · synced Jun 8, 2026