gudid
Primary ID: 20132-256
ERBE (UDI 20132-256)
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 20132-256
Device Regulatory Overview
The ERBE (Model/Catalog Number: 20132-256) 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
- 20132-256
- Product Code / EMDN
- GEI
- Device Name
- Database Sync Date
- 2026-08-09 09:11:21
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 20132-256.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint