eudamed_udi
Primary ID: E0HMKTB031
myplant (UDI E0HMKTB031)
Manufactured by Hager & Meisinger GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for myplant - Primary ID E0HMKTB031
Device Regulatory Overview
The myplant (Model/Catalog Number: KTB03) is a medical device manufactured by Hager & Meisinger GmbH. This product is indexed under FDA Product Code / Category Classification P01020180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KTB03
- Product Code / EMDN
- P01020180
- Device Name
- Prosthetic abutment systems
- Database Sync Date
- 2026-08-09 16:29:36
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 myplant?
The registered manufacturer of record for myplant is Hager & Meisinger GmbH.
What is the Primary UDI-DI identifier for myplant?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E0HMKTB031.
What classification code is assigned to this device?
This device is registered under product classification code P01020180.
Similar Classification Devices (P01020180)
Other Devices by Hager & Meisinger GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint