gudid
Primary ID: FC-GRAN-002
Resilience (UDI FC-GRAN-002)
Manufactured by ORTHO TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Resilience - Primary ID FC-GRAN-002
Device Regulatory Overview
The Resilience (Model/Catalog Number: FC-GRAN-002) is a medical device manufactured by ORTHO TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FC-GRAN-002
- Product Code / EMDN
- EMA
- Device Name
- Powder/Liq Ionomer Starter Kit 50gm powder and 50mL liquid
- Database Sync Date
- 2026-08-09 09:00:52
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 Resilience?
The registered manufacturer of record for Resilience is ORTHO TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for Resilience?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FC-GRAN-002.
What classification code is assigned to this device?
This device is registered under product classification code EMA.
Similar Classification Devices (EMA)
Other Devices by ORTHO TECHNOLOGY, INC.
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