GUDIDData
gudid Primary ID: MT600TS

Forest (UDI MT600TS)

Manufactured by Ls Enterprises, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Forest - Primary ID MT600TS

Device Regulatory Overview

The Forest (Model/Catalog Number: MT600TS) is a medical device manufactured by Ls Enterprises, Inc.. This product is indexed under FDA Product Code / Category Classification EIA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MT600TS
Product Code / EMDN
EIA
Device Name
DR'S TOP SHELF MOUNT, MT COMPACT CONTROL, 3-HANDPIECE AUTOMATIC
Database Sync Date
2026-08-09 09:02:00

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 Forest?

The registered manufacturer of record for Forest is Ls Enterprises, Inc..

What is the Primary UDI-DI identifier for Forest?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MT600TS.

What classification code is assigned to this device?

This device is registered under product classification code EIA.

Programmatic Export

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

JSON API Endpoint