gudid
Primary ID: 8601INT
Forest (UDI 8601INT)
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 8601INT
Device Regulatory Overview
The Forest (Model/Catalog Number: 8601INT) 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
- 8601INT
- Product Code / EMDN
- EIA
- Device Name
- PIVOT ARM W/CHAIR ADAPTER & WATER SYSTEM
- Database Sync Date
- 2026-08-09 09:02:00
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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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 8601INT.
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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