gudid
Primary ID: GB30
JITTO (UDI GB30)
Manufactured by GALEMED CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JITTO - Primary ID GB30
Device Regulatory Overview
The JITTO (Model/Catalog Number: GB30) is a medical device manufactured by GALEMED CORPORATION. This product is indexed under FDA Product Code / Category Classification CAP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GB30
- Product Code / EMDN
- CAP
- Device Name
- Database Sync Date
- 2026-08-09 09:15:32
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 JITTO?
The registered manufacturer of record for JITTO is GALEMED CORPORATION.
What is the Primary UDI-DI identifier for JITTO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GB30.
What classification code is assigned to this device?
This device is registered under product classification code CAP.
Similar Classification Devices (CAP)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint