eudamed_udi
Primary ID: 00195893307609
Veinlite EMS PRO DPC (UDI 00195893307609)
Manufactured by Translite, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Veinlite EMS PRO DPC - Primary ID 00195893307609
Device Regulatory Overview
The Veinlite EMS PRO DPC (Model/Catalog Number: VEMS-DPC) is a medical device manufactured by Translite, LLC. This product is indexed under FDA Product Code / Category Classification T030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VEMS-DPC
- Product Code / EMDN
- T030199
- Device Name
- Veinlite EMS PRO DPC
- Database Sync Date
- 2026-08-09 18:15:57
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 Veinlite EMS PRO DPC?
The registered manufacturer of record for Veinlite EMS PRO DPC is Translite, LLC.
What is the Primary UDI-DI identifier for Veinlite EMS PRO DPC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00195893307609.
What classification code is assigned to this device?
This device is registered under product classification code T030199.
Similar Classification Devices (T030199)
Other Devices by Translite, LLC
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