Identity
- Trade Name
- DermLite Carbon FDA UDI
- Generic Name
- Dermatoscope, optical FDA UDI
- Device Name
- Handheld dermatoscope (battery-operated, polarized, non-polarized, snap-on spacer) FDA UDI
- Model / Reference
- DLC FDA UDI
- Description
- Handheld dermatoscope (battery-operated, polarized, non-polarized, snap-on spacer) FDA UDI
Identifiers
- Catalog Number
- DLC FDA UDI
- Primary DI / UDI-DI
- 00855997006319 FDA UDI
- FDA Product Code
- KYT FDA UDI
- GMDN Term
- Dermatoscope, optical FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6350 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dermatoscope, optical
DermLite Carbon by DermLite LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dermatoscope, optical.
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- Diagnostix™ — American Diagnostic Corporation · Class I
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- HEINE diSTANCE — Heine Optotechnik GmbH & Co. KG · Class I
- Diagnostix™ — American Diagnostic Corporation · Class I
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
- DermLite LLC
Sources (1)
- FDA UDI 5aa26854-1581-42b2-a2ed-d951074cf29f 35 fields · synced May 31, 2026