eudamed_udi
Primary ID: E0HM45001767220201
Unspecified Brand (UDI E0HM45001767220201)
Manufactured by Hager & Meisinger GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID E0HM45001767220201
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 4500176722020) is a medical device manufactured by Hager & Meisinger GmbH. This product is indexed under FDA Product Code / Category Classification Q0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4500176722020
- Product Code / EMDN
- Q0199
- Device Name
- Surgical hand-held instruments
- Database Sync Date
- 2026-08-09 16:46:45
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Hager & Meisinger GmbH.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E0HM45001767220201.
What classification code is assigned to this device?
This device is registered under product classification code Q0199.
Similar Classification Devices (Q0199)
Other Devices by Hager & Meisinger GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint