eudamed_udi
Primary ID: E0HM504112BL1
OKTAGON (UDI E0HM504112BL1)
Manufactured by Hager & Meisinger GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OKTAGON - Primary ID E0HM504112BL1
Device Regulatory Overview
The OKTAGON (Model/Catalog Number: 504112BL) is a medical device manufactured by Hager & Meisinger GmbH. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 504112BL
- Product Code / EMDN
- P01020101
- Device Name
- Oktagon Dental Implants
- Database Sync Date
- 2026-08-09 16:46:24
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 OKTAGON?
The registered manufacturer of record for OKTAGON is Hager & Meisinger GmbH.
What is the Primary UDI-DI identifier for OKTAGON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E0HM504112BL1.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
Other Devices by Hager & Meisinger GmbH
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