gudid
Primary ID: 20402-401
ERBE (UDI 20402-401)
Manufactured by Erbe Elektromedizin GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERBE - Primary ID 20402-401
Device Regulatory Overview
The ERBE (Model/Catalog Number: 20402-401) is a medical device manufactured by Erbe Elektromedizin GmbH. This product is indexed under FDA Product Code / Category Classification GEH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20402-401
- Product Code / EMDN
- GEH
- Device Name
- Database Sync Date
- 2026-08-09 09:11:21
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 ERBE?
The registered manufacturer of record for ERBE is Erbe Elektromedizin GmbH.
What is the Primary UDI-DI identifier for ERBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20402-401.
What classification code is assigned to this device?
This device is registered under product classification code GEH.
Similar Classification Devices (GEH)
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