Unspecified Brand (UDI 08053470218828)
Manufactured by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: TGK.4080S) is a medical device manufactured by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.. This product is indexed under FDA Product Code / Category Classification P09120603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TGK.4080S
- Product Code / EMDN
- P09120603
- Device Name
- Cannulated Large Diameter Self-Tapping Self-Drilling Osteosynthesis Screw
- Database Sync Date
- 2026-08-09 16:28:45
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053470218828.
What classification code is assigned to this device?
This device is registered under product classification code P09120603.
Similar Classification Devices (P09120603)
Other Devices by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint