gudid
Primary ID: D201045
GRAFTSITE (UDI D201045)
Manufactured by SUMMIT MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GRAFTSITE - Primary ID D201045
Device Regulatory Overview
The GRAFTSITE (Model/Catalog Number: D201045) is a medical device manufactured by SUMMIT MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification CAZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D201045
- Product Code / EMDN
- CAZ
- Device Name
- GRAFTSITE Delivery Assistance Device
- Database Sync Date
- 2026-08-09 09:22:51
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 GRAFTSITE?
The registered manufacturer of record for GRAFTSITE is SUMMIT MEDICAL LIMITED.
What is the Primary UDI-DI identifier for GRAFTSITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D201045.
What classification code is assigned to this device?
This device is registered under product classification code CAZ.
Similar Classification Devices (CAZ)
Other Devices by SUMMIT MEDICAL LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint