Identity
- Trade Name
- ReActiv8 Programming Wand FDA UDI
- Generic Name
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer FDA UDI
- Device Name
- Programming Wand FDA UDI
- Model / Reference
- 6M6000-002 FDA UDI
- Description
- Programming Wand FDA UDI
Identifiers
- Catalog Number
- 6000 FDA UDI
- Primary DI / UDI-DI
- 05391527770213 FDA UDI
- PMA Number
- P190021 FDA UDI
- FDA Product Code
- QLK FDA UDI
- GMDN Term
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer
ReActiv8 Programming Wand by Mainstay Medical Limited — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer.
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Cleared under the same submission
P190021 also covers:
- Mainstay Tunneler — MAINSTAY MEDICAL LIMITED
- ReActiv8 Activator — MAINSTAY MEDICAL LIMITED
- ReActiv8 IPG — MAINSTAY MEDICAL LIMITED
- ReActiv8 Magnet — MAINSTAY MEDICAL LIMITED
- ReActiv8 Programmer — MAINSTAY MEDICAL LIMITED
- ReActiv8 Programmer — MAINSTAY MEDICAL LIMITED
- ReActiv8 Stimulation Lead — MAINSTAY MEDICAL LIMITED
- ReActiv8 Stimulation Lead — MAINSTAY MEDICAL LIMITED
- ReActiv8 Torque Wrench — MAINSTAY MEDICAL LIMITED
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
- Mainstay Medical Limited
Sources (1)
- FDA UDI 9bacf3a2-f7fe-49c2-ab49-50d3f8509934 36 fields · synced May 30, 2026