← Back to catalogue
DermLite Universal Smartphone Adapter
FDA UDIClass I (US FDA UDI)
by DermLite LLC
Identity
- Trade Name
- DermLite Universal Smartphone Adapter FDA UDI
- Generic Name
- Dermatoscope, optical FDA UDI
- Device Name
- Universal clamp-style smartphone adapter for attaching compatible DL models FDA UDI
- Model / Reference
- DLUA FDA UDI
- Description
- Universal clamp-style smartphone adapter for attaching compatible DL models FDA UDI
Identifiers
- Catalog Number
- DLUA FDA UDI
- Primary DI / UDI-DI
- 00855997006111 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 Universal Smartphone Adapter by DermLite LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dermatoscope, optical.
- Diagnostix™ — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class I
- Diagnostix™ — American Diagnostic Corporation · Class I
- Diagnostix™ — American Diagnostic Corporation · Class I
- Diagnostix™ — American Diagnostic Corporation · Class I
- Diagnostix™ — American Diagnostic Corporation · Class I
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- DermLite LLC
Sources (1)
- FDA UDI 872e2700-d2d3-462d-bb9b-5d5f9c874070 35 fields · synced Jun 8, 2026