eudamed_udi
Primary ID: 07611819349452
PFNA (UDI 07611819349452)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PFNA - Primary ID 07611819349452
Device Regulatory Overview
The PFNA (Model/Catalog Number: 03.010.408) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03.010.408
- Product Code / EMDN
- L091001
- Device Name
- Orthopaedic Aiming Devices
- Database Sync Date
- 2026-08-09 16:28:56
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 PFNA?
The registered manufacturer of record for PFNA is Synthes GmbH.
What is the Primary UDI-DI identifier for PFNA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819349452.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
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