Identity
- Trade Name
- MedLED Spectra FDA UDI
- Generic Name
- Head-worn lamp FDA UDI
- Device Name
- Standard Kit FDA UDI
- Model / Reference
- MG3-SK FDA UDI
- Description
- Standard Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810020080704 FDA UDI
- FDA Product Code
- HPP FDA UDI
- GMDN Term
- Head-worn lamp FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4335 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
Yes
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
Yes
FDA UDI
Category: Noninvasive device battery chargerHead-worn lampSecondary battery
MedLED Spectra by Riverpoint Medical Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Riverpoint Medical Llc
Sources (1)
- FDA UDI 72dd7f23-1f16-4eff-8bef-6ee6e3ef376a 33 fields · synced May 30, 2026