Identity
- Trade Name
- Nervo-Scope FDA UDI
- Generic Name
- Intermittent electronic patient thermometer FDA UDI
- Device Name
- A thermal detection instrument for chiropractic professionals that detects and measures minute heat differences in the tissues along the spine. This model is equipped with a port for an external graphing printer and control buttons for the printer. FDA UDI
- Model / Reference
- ETS-9A FDA UDI
- Description
- A thermal detection instrument for chiropractic professionals that detects and measures minute heat differences in the tissues along the spine. This model is equipped with a port for an external graphing printer and control buttons for the printer. FDA UDI
Identifiers
- Catalog Number
- ETS-9A FDA UDI
- Primary DI / UDI-DI
- B381ETS9A0 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Intermittent electronic patient thermometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 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
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Intermittent electronic patient thermometer
Nervo-Scope by Electronic Development Laboratories, 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
- Electronic Development Laboratories, Inc.
Sources (1)
- FDA UDI 2f8925f9-0c39-423e-a2ff-a5cbe9a5a1fd 35 fields · synced May 30, 2026