gudid
Primary ID: 7010UC-C
Forest (UDI 7010UC-C)
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 7010UC-C
Device Regulatory Overview
The Forest (Model/Catalog Number: 7010UC-C) 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
- 7010UC-C
- Product Code / EMDN
- EIA
- Device Name
- DUO SYSTEM, REAR MOUNT, UNDER CABINET FLOOR MOUNT SIDE DELIVERY W/SOLID SURFACE TOP, DESIGNER FRIENDLY
- 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
}
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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 7010UC-C.
What classification code is assigned to this device?
This device is registered under product classification code EIA.
Similar Classification Devices (EIA)
Other Devices by Ls Enterprises, Inc.
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