gudid
Primary ID: SGP200
StarGraft Putty (UDI SGP200)
Manufactured by COLLAGEN MATRIX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for StarGraft Putty - Primary ID SGP200
Device Regulatory Overview
The StarGraft Putty (Model/Catalog Number: SGP200) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification NPM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SGP200
- Product Code / EMDN
- NPM
- Device Name
- Synthetic Mineral Collagen Composite Bone Graft
- Database Sync Date
- 2026-08-09 09:14:39
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 StarGraft Putty?
The registered manufacturer of record for StarGraft Putty is COLLAGEN MATRIX, INC..
What is the Primary UDI-DI identifier for StarGraft Putty?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SGP200.
What classification code is assigned to this device?
This device is registered under product classification code NPM.
Similar Classification Devices (NPM)
Other Devices by COLLAGEN MATRIX, INC.
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