AYSAM (UDI 08684543857271)
Manufactured by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi
Device Regulatory Overview
The AYSAM (Model/Catalog Number: A3385460) is a medical device manufactured by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi. This product is indexed under FDA Product Code / Category Classification P09120201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A3385460
- Product Code / EMDN
- P09120201
- Device Name
- R PROXIMAL FEMUR KANULLU TITANYUM UZUN CIVI SOL (R PROXIMAL FEMUR CANNULATED TITANIUM LONG NAIL LEFT) 15 X 460 MM
- 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 AYSAM?
The registered manufacturer of record for AYSAM is Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi.
What is the Primary UDI-DI identifier for AYSAM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684543857271.
What classification code is assigned to this device?
This device is registered under product classification code P09120201.
Similar Classification Devices (P09120201)
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