Identity
- Trade Name
- LUMINDEX FDA UDI
- Generic Name
- Fixed examination/treatment room light FDA UDI
- Device Name
- LUMINDEX 5 (US) FDA UDI
- Model / Reference
- LUMINDEX 5 FDA UDI
- Description
- LUMINDEX 5 (US) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719873921461 FDA UDI
- FDA Product Code
- HPP FDA UDI
- GMDN Term
- Fixed examination/treatment room light 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
Yes
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
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: Fixed examination/treatment room light
Lumindex by Dentmate Technology Co. , Ltd. — 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
- Dentmate Technology Co. , Ltd.
Sources (1)
- FDA UDI 78b5b903-bee8-4e9a-a63e-c316f4619194 33 fields · synced Jun 1, 2026