gudid
Primary ID: GM11013800
Aarhus Applicator Set (UDI GM11013800)
Manufactured by VARIAN MEDICAL SYSTEMS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aarhus Applicator Set - Primary ID GM11013800
Device Regulatory Overview
The Aarhus Applicator Set (Model/Catalog Number: GM11013800) is a medical device manufactured by VARIAN MEDICAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification JAQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GM11013800
- Product Code / EMDN
- JAQ
- Device Name
- Contains: GM11013810-00816389028036, GM11013820-00816389028043
- Database Sync Date
- 2026-08-09 09:22:18
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 Aarhus Applicator Set?
The registered manufacturer of record for Aarhus Applicator Set is VARIAN MEDICAL SYSTEMS, INC..
What is the Primary UDI-DI identifier for Aarhus Applicator Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GM11013800.
What classification code is assigned to this device?
This device is registered under product classification code JAQ.
Similar Classification Devices (JAQ)
Other Devices by VARIAN MEDICAL SYSTEMS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint