gudid
Primary ID: GLOBUS REVO STC
GLOBUS (UDI GLOBUS REVO STC)
Manufactured by DOMINO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GLOBUS - Primary ID GLOBUS REVO STC
Device Regulatory Overview
The GLOBUS (Model/Catalog Number: GLOBUS REVO STC) is a medical device manufactured by DOMINO SRL. This product is indexed under FDA Product Code / Category Classification GZJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GLOBUS REVO STC
- Product Code / EMDN
- GZJ
- Device Name
- The Globus Device is a programmable electro stimulator with multiple uses: Powered Muscle Stimulators, Transcutaneous Electrical Nerve Stimulator.Premodulated Current Therapy Stimulator, and Microcurrent Therapy Stimulator.
- Database Sync Date
- 2026-08-09 09:05:06
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 GLOBUS?
The registered manufacturer of record for GLOBUS is DOMINO SRL.
What is the Primary UDI-DI identifier for GLOBUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GLOBUS REVO STC.
What classification code is assigned to this device?
This device is registered under product classification code GZJ.
Similar Classification Devices (GZJ)
Other Devices by DOMINO SRL
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