Identity
- Trade Name
- Symplicity G3™ EUDAMEDFDA UDI
- Generic Name
- Percutaneous radio-frequency ablation system generator FDA UDI
- Device Name
- Symplicity G3 Generator EUDAMEDGENERATOR RDNG3A G3SV5.1 US JP CA FDA UDI
- Model / Reference
- RDNG3A EUDAMEDFDA UDI
- Description
- GENERATOR RDNG3A G3SV5.1 US JP CA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000688288 EUDAMED00763000688226 EUDAMED00763000688264 EUDAMED00763000688189 EUDAMED00763000688325 EUDAMED00763000688356 EUDAMED00763000688301 EUDAMED00763000688240 EUDAMED00763000688318 EUDAMED00763000387020 FDA UDI
- Basic UDI-DI
- 0763000B00019178K EUDAMED
- PMA Number
- P220026 FDA UDI
- FDA Product Code
- QYI FDA UDI
- EMDN Code
- K0299 ELECTROSURGERY DEVICES, SINGLE-USE - OTHER EUDAMED
- GMDN Term
- Percutaneous radio-frequency ablation system generator FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass III FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
Yes
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Percutaneous radio-frequency ablation system generator
Symplicity G3™ by Medtronic, Inc. — Class III — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Percutaneous radio-frequency ablation system generator.
- OneRF Ablation System — NEUROONE MEDICAL TECHNOLOGIES CORP. · Class II
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- Maestro 4000™ Controller — Boston Scientific · Class III
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Cleared under the same submission
P220026 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class III | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (11)
- FDA UDI 72f1e5f2-9e8c-417d-835c-c51550711ea5 36 fields · synced Aug 5, 2026
- EUDAMED 420ef516-68f4-4519-a759-f03a4ba369ac 61 fields · synced Jul 8, 2026
- EUDAMED a31e6270-a5cf-4339-b94e-18169da7c2c1 61 fields · synced Jul 10, 2026
- EUDAMED 3a06179c-e83e-41f8-9b2e-c9f88f8165ca 61 fields · synced Jul 15, 2026
- EUDAMED 2a3372bb-4af4-4366-b812-fd732b58b1a0 61 fields · synced Jul 15, 2026
- EUDAMED 40736a02-0455-4971-b8a8-e3ff0608f1f1 61 fields · synced Jul 18, 2026
- EUDAMED 6a1b0134-4d7c-40bb-8b4a-c0bc7e8b5482 61 fields · synced Jul 28, 2026
- EUDAMED 04c5bd5c-8197-469f-8ffe-ab7e9fc4a2f6 61 fields · synced Aug 1, 2026
- EUDAMED 7c10ed72-a2e5-4fca-8ce6-923bffec762c 61 fields · synced Aug 2, 2026
- EUDAMED 1d52ef43-f258-4845-ab44-a751a94c8ffa 61 fields · synced Aug 3, 2026
- EUDAMED 1cc17035-1435-49d9-9394-44bdd81e0117 61 fields · synced Aug 5, 2026