Identity
- Trade Name
- Neuroglide FDA UDI
- Generic Name
- Bed/chair electric massager FDA UDI
- Device Name
- Controller Unit for the Neuroglide Pain Relief and Recovery System. FDA UDI
- Model / Reference
- T162020 FDA UDI
- Description
- Controller Unit for the Neuroglide Pain Relief and Recovery System. FDA UDI
Identifiers
- Catalog Number
- A-00100 FDA UDI
- Primary DI / UDI-DI
- G067T1620200 FDA UDI
- 510(k) Number
- K202693 FDA UDI
- FDA Product Code
- IRP FDA UDI
- GMDN Term
- Bed/chair electric massager FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5650 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
No
FDA UDI
Over-the-Counter
Yes
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
Category: Bed/chair electric massager
Neuroglide by Eva Medtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K202693 also covers:
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
- Eva Medtec, Inc.
Sources (1)
- FDA UDI 810e45d2-867c-4dc6-9689-f1842b5e88bc 35 fields · synced May 31, 2026