eudamed_udi
Primary ID: 04050147006072
Bipolare Pinzette; gerade (UDI 04050147006072)
Manufactured by Erbe Elektromedizin GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bipolare Pinzette; gerade - Primary ID 04050147006072
Device Regulatory Overview
The Bipolare Pinzette; gerade (Model/Catalog Number: 20195-098) is a medical device manufactured by Erbe Elektromedizin GmbH. This product is indexed under FDA Product Code / Category Classification L180401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20195-098
- Product Code / EMDN
- L180401
- Device Name
- Bipolar forceps, RU
- Database Sync Date
- 2026-08-09 16:30:30
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 Bipolare Pinzette; gerade?
The registered manufacturer of record for Bipolare Pinzette; gerade is Erbe Elektromedizin GmbH.
What is the Primary UDI-DI identifier for Bipolare Pinzette; gerade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050147006072.
What classification code is assigned to this device?
This device is registered under product classification code L180401.
Similar Classification Devices (L180401)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint