eudamed_udi
Primary ID: 07611819759718
STARDRIVE (UDI 07611819759718)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STARDRIVE - Primary ID 07611819759718
Device Regulatory Overview
The STARDRIVE (Model/Catalog Number: 201.370) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification P09120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201.370
- Product Code / EMDN
- P09120601
- Device Name
- Cortex Screw Stainless Steel
- Database Sync Date
- 2026-08-09 16:28:44
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 STARDRIVE?
The registered manufacturer of record for STARDRIVE is Synthes GmbH.
What is the Primary UDI-DI identifier for STARDRIVE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819759718.
What classification code is assigned to this device?
This device is registered under product classification code P09120601.
Similar Classification Devices (P09120601)
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