eudamed_udi
Primary ID: 1311813HG300VF179
Haltegriff 300 mm, Fingergriff, verdeckte Montage (UDI 1311813HG300VF179)
Manufactured by FRELU GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Haltegriff 300 mm, Fingergriff, verdeckte Montage - Primary ID 1311813HG300VF179
Device Regulatory Overview
The Haltegriff 300 mm, Fingergriff, verdeckte Montage (Model/Catalog Number: HG300VF) is a medical device manufactured by FRELU GmbH. This product is indexed under FDA Product Code / Category Classification Y181803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HG300VF
- Product Code / EMDN
- Y181803
- Device Name
- Haltegriffe
- Database Sync Date
- 2026-08-09 16:48:33
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 Haltegriff 300 mm, Fingergriff, verdeckte Montage?
The registered manufacturer of record for Haltegriff 300 mm, Fingergriff, verdeckte Montage is FRELU GmbH.
What is the Primary UDI-DI identifier for Haltegriff 300 mm, Fingergriff, verdeckte Montage?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1311813HG300VF179.
What classification code is assigned to this device?
This device is registered under product classification code Y181803.
Similar Classification Devices (Y181803)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint