gudid
Primary ID: E1-WB
E100 series(E1-M, E1-C, E1-W) (UDI E1-WB)
Manufactured by DENTIS CO. ,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for E100 series(E1-M, E1-C, E1-W) - Primary ID E1-WB
Device Regulatory Overview
The E100 series(E1-M, E1-C, E1-W) (Model/Catalog Number: E1-WB) is a medical device manufactured by DENTIS CO. ,LTD. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E1-WB
- Product Code / EMDN
- KZF
- Device Name
- INPUT : DC 15 V, 1.67 A AC/DC Adaptor : Glob Tek, Inc./GRM41060-33
- Database Sync Date
- 2026-08-09 09:13:00
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 E100 series(E1-M, E1-C, E1-W)?
The registered manufacturer of record for E100 series(E1-M, E1-C, E1-W) is DENTIS CO. ,LTD.
What is the Primary UDI-DI identifier for E100 series(E1-M, E1-C, E1-W)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E1-WB.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by DENTIS CO. ,LTD
Programmatic Export
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