gudid
Primary ID: 447.62
NA (UDI 447.62)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 447.62
Device Regulatory Overview
The NA (Model/Catalog Number: 447.62) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification GXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 447.62
- Product Code / EMDN
- GXR
- Device Name
- 2.0MM TI Y-PLATE 2 X 4 HOLES
- Database Sync Date
- 2026-08-09 09:39:06
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 NA?
The registered manufacturer of record for NA is Synthes GmbH.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 447.62.
What classification code is assigned to this device?
This device is registered under product classification code GXR.
Similar Classification Devices (GXR)
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