eudamed_udi
Primary ID: 08905926005547
Kaushik (UDI 08905926005547)
Manufactured by Kaushik Orthopaedic Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kaushik - Primary ID 08905926005547
Device Regulatory Overview
The Kaushik (Model/Catalog Number: KNLB-T-6.5-055) is a medical device manufactured by Kaushik Orthopaedic Private Limited. This product is indexed under FDA Product Code / Category Classification P09120604 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KNLB-T-6.5-055
- Product Code / EMDN
- P09120604
- Device Name
- traumaHeal Locking Bolt 6.5mm, Cannulated, Self-Tapping, Length 55mm, Titanium
- Database Sync Date
- 2026-08-09 16:29:23
Full Regulatory Attributes
đź”’ Token Gated
{
"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 Kaushik?
The registered manufacturer of record for Kaushik is Kaushik Orthopaedic Private Limited.
What is the Primary UDI-DI identifier for Kaushik?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08905926005547.
What classification code is assigned to this device?
This device is registered under product classification code P09120604.
Similar Classification Devices (P09120604)
Other Devices by Kaushik Orthopaedic Private Limited
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