gudid
Primary ID: MED-USG-CLEAR-8.5OZ-A
MedVat (UDI MED-USG-CLEAR-8.5OZ-A)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MedVat - Primary ID MED-USG-CLEAR-8.5OZ-A
Device Regulatory Overview
The MedVat (Model/Catalog Number: MED-USG-CLEAR-8.5OZ-A) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification MUI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MED-USG-CLEAR-8.5OZ-A
- Product Code / EMDN
- MUI
- Device Name
- Ultrasonic Gel with Aloe Vera
- Database Sync Date
- 2026-08-09 09:49:29
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 MedVat?
The registered manufacturer of record for MedVat is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for MedVat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MED-USG-CLEAR-8.5OZ-A.
What classification code is assigned to this device?
This device is registered under product classification code MUI.
Similar Classification Devices (MUI)
Other Devices by PARKER LABORATORIES INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint