gudid
Primary ID: 5081
GUIDOR (UDI 5081)
Manufactured by SUNSTAR AMERICAS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUIDOR - Primary ID 5081
Device Regulatory Overview
The GUIDOR (Model/Catalog Number: 5081) is a medical device manufactured by SUNSTAR AMERICAS, INC.. This product is indexed under FDA Product Code / Category Classification NPK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5081
- Product Code / EMDN
- NPK
- Device Name
- GUIDOR Bioresorbable Matrix Barrier
- Database Sync Date
- 2026-08-09 09:08:47
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 GUIDOR?
The registered manufacturer of record for GUIDOR is SUNSTAR AMERICAS, INC..
What is the Primary UDI-DI identifier for GUIDOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5081.
What classification code is assigned to this device?
This device is registered under product classification code NPK.
Similar Classification Devices (NPK)
Other Devices by SUNSTAR AMERICAS, INC.
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