gudid
Primary ID: 20132-257
Erbe (UDI 20132-257)
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 20132-257
Device Regulatory Overview
The Erbe (Model/Catalog Number: 20132-257) is a medical device manufactured by Erbe Elektromedizin GmbH. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20132-257
- Product Code / EMDN
- GEI
- 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 20132-257.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
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