gudid
Primary ID: 901134
GRADIA (UDI 901134)
Manufactured by Gc America Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GRADIA - Primary ID 901134
Device Regulatory Overview
The GRADIA (Model/Catalog Number: 901134) is a medical device manufactured by Gc America Inc.. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 901134
- Product Code / EMDN
- EBF
- Device Name
- GRADIA PLUS DTip Ntype LP Cover 5pc
- Database Sync Date
- 2026-08-09 09:02:01
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 GRADIA?
The registered manufacturer of record for GRADIA is Gc America Inc..
What is the Primary UDI-DI identifier for GRADIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 901134.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
Other Devices by Gc America Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint