gudid Primary ID: VTS1000-CB

Syris v900L Charging Base (UDI VTS1000-CB)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Syris v900L Charging Base (Model/Catalog Number: VTS1000-CB) 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...

🔒 Compromised Lot & Serial Numbers Locked

Verify if facility inventory is affected by this recall.

Unlock Lot Data ($49)

Technical Specifications

Model Number: VTS1000-CB
Product Code / EMDN: KYT
Device Name: Syris v900L Charging Base
Database Sync Date: 2026-08-09 09:37:45

Full Regulatory Attributes

🔒 Token Gated

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Syris v900L Charging Base?

The registered manufacturer of record for Syris v900L Charging Base is DermLite LLC.

What is the Primary UDI-DI identifier for Syris v900L Charging Base?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VTS1000-CB.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint