eudamed_udi
Primary ID: 07611819766761
Unspecified Brand (UDI 07611819766761)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 07611819766761
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 388.654) 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
- 388.654
- Product Code / EMDN
- L091001
- Device Name
- Extractor Extender Screwdriver Shaft Ratchet T-Handle Torque-limiting Handle Rod Bender Remobilization Tool Handle Bending Iron Sleeve In-situ Bender Rod Pusher Extraction Pliers Ratchet Counter Torque Screwdriver
- Database Sync Date
- 2026-08-09 16:28:50
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Synthes GmbH.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819766761.
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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