gudid Primary ID: DLCKi14PM

DL Connection Kit for iPhone 14 Pro Max (UDI DLCKi14PM)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The DL Connection Kit for iPhone 14 Pro Max (Model/Catalog Number: DLCKi14PM) is a medical device manufactured by DermLite LLC. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1506-2023 View Full Alert →

DERMLITE DL4W, REF: DL4W, Rx Only MD, CE...

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Technical Specifications

Model Number: DLCKi14PM
Product Code / EMDN: KYT
Device Name: Smartphone case with magnetic connection for compatible DL models
Database Sync Date: 2026-08-09 09:37:45

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of DL Connection Kit for iPhone 14 Pro Max?

The registered manufacturer of record for DL Connection Kit for iPhone 14 Pro Max is DermLite LLC.

What is the Primary UDI-DI identifier for DL Connection Kit for iPhone 14 Pro Max?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DLCKi14PM.

What classification code is assigned to this device?

This device is registered under product classification code KYT.

Similar Classification Devices (KYT)

Other Devices by DermLite LLC

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