Identity
- Trade Name
- VQ OrthoCare FDA UDI
- Generic Name
- Interferential electrical stimulation system FDA UDI
- Device Name
- Avid IF2 INTERFERENTIAL STIMULATION SYSTEM FDA UDI
- Model / Reference
- AV-IF19A FDA UDI
- Description
- Avid IF2 INTERFERENTIAL STIMULATION SYSTEM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817717021811 FDA UDI
- 510(k) Number
- K183692 FDA UDI
- FDA Product Code
- NYN FDA UDI
- GMDN Term
- Interferential electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 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
Yes
FDA UDI
Category: Interferential electrical stimulation system
VQ OrthoCare by Vision Quest Industries Incorporated — 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
- Vision Quest Industries Incorporated
Sources (1)
- FDA UDI f1479af2-ba0d-4976-b8bd-378b94cd2f10 35 fields · synced May 30, 2026