← Back to catalogue

MagnetiConnect Kit - Smartphone/Tablet Adapter

FDA UDI

Class I (US FDA UDI)

by DermLite LLC

Identity

Trade Name
MagnetiConnect Kit - Smartphone/Tablet Adapter FDA UDI
Generic Name
Dermatoscope, optical FDA UDI
Device Name
Adhesive connectors to attach compatible DL models to smartphone & tablets FDA UDI
Model / Reference
MCK FDA UDI
Description
Adhesive connectors to attach compatible DL models to smartphone & tablets FDA UDI

Identifiers

Catalog Number
MCK FDA UDI
Primary DI / UDI-DI
00855997006678 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

MagnetiConnect Kit - Smartphone/Tablet Adapter by DermLite LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatoscope, optical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
DermLite LLC

Sources (1)

  • FDA UDI b245224c-1fe4-49f7-8bc2-bc8e7217a0f2 35 fields · synced May 30, 2026