eudamed_udi
Primary ID: 00842326185005
Myerson GanyMed (UDI 00842326185005)
Manufactured by The Myerson Company Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Myerson GanyMed - Primary ID 00842326185005
Device Regulatory Overview
The Myerson GanyMed (Model/Catalog Number: T92B3L0032) is a medical device manufactured by The Myerson Company Limited. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T92B3L0032
- Product Code / EMDN
- P01020101
- Device Name
- Preformed Artificial Teeth
- Database Sync Date
- 2026-08-09 16:28:46
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 Myerson GanyMed?
The registered manufacturer of record for Myerson GanyMed is The Myerson Company Limited.
What is the Primary UDI-DI identifier for Myerson GanyMed?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842326185005.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
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