eudamed_udi
Primary ID: 06973596010200
Vista Plus (UDI 06973596010200)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vista Plus - Primary ID 06973596010200
Device Regulatory Overview
The Vista Plus (Model/Catalog Number: TRANS2) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification W0202030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TRANS2
- Product Code / EMDN
- W0202030202
- Device Name
- Vista Plus
- Database Sync Date
- 2026-08-09 18:46:25
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 Vista Plus?
The registered manufacturer of record for Vista Plus is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Vista Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010200.
What classification code is assigned to this device?
This device is registered under product classification code W0202030202.
Similar Classification Devices (W0202030202)
Other Devices by Conlett Technology Inc
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