Identity
- Trade Name
- NQ TMS Applicator FDA UDI
- Generic Name
- Magnetic neural stimulation system FDA UDI
- Device Name
- Coil or Applicator: It is used with a Transcranial Magnetic Stimulator (TMS) to generate a magnetic field that in turn delivers electrical stimulation to the patient’s cortex. It is positioned to target a specific stimulation region of interest. FDA UDI
- Model / Reference
- NQv1-AC-01 FDA UDI
- Description
- Coil or Applicator: It is used with a Transcranial Magnetic Stimulator (TMS) to generate a magnetic field that in turn delivers electrical stimulation to the patient’s cortex. It is positioned to target a specific stimulation region of interest. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860012355426 FDA UDI
- FDA Product Code
- OBP FDA UDI
- GMDN Term
- Magnetic neural stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5805 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Magnetic neural stimulation system
NQ TMS Applicator by Neuroqore, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Neuroqore, Inc.
Sources (1)
- FDA UDI 0d821f4f-4912-4e71-891e-c0594bdeadf5 34 fields · synced Jun 1, 2026