eudamed_udi
Primary ID: 08903424372062
Tynor (UDI 08903424372062)
Manufactured by Tynor Orthotics Pvt Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tynor - Primary ID 08903424372062
Device Regulatory Overview
The Tynor (Model/Catalog Number: A 06) is a medical device manufactured by Tynor Orthotics Pvt Ltd. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A 06
- Product Code / EMDN
- Y060309
- Device Name
- Orthosis,Thoracolumbosacral Spine
- Database Sync Date
- 2026-08-09 16:29:17
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 Tynor?
The registered manufacturer of record for Tynor is Tynor Orthotics Pvt Ltd.
What is the Primary UDI-DI identifier for Tynor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08903424372062.
What classification code is assigned to this device?
This device is registered under product classification code Y060309.
Similar Classification Devices (Y060309)
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