Myerson DB Plus Composite (UDI 00842326139572)
Manufactured by The Myerson Company Limited
Device Regulatory Overview
The Myerson DB Plus Composite (Model/Catalog Number: T34D2U0F35) 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
- T34D2U0F35
- Product Code / EMDN
- P01020101
- Device Name
- Preformed Artificial Teeth
- Database Sync Date
- 2026-08-09 16:28:47
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 DB Plus Composite?
The registered manufacturer of record for Myerson DB Plus Composite is The Myerson Company Limited.
What is the Primary UDI-DI identifier for Myerson DB Plus Composite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842326139572.
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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