gudid
Primary ID: ZLR3006
NVPRO3 (UDI ZLR3006)
Manufactured by DEN-MAT HOLDINGS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NVPRO3 - Primary ID ZLR3006
Device Regulatory Overview
The NVPRO3 (Model/Catalog Number: ZLR3006) is a medical device manufactured by DEN-MAT HOLDINGS, LLC. This product is indexed under FDA Product Code / Category Classification GEX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZLR3006
- Product Code / EMDN
- GEX
- Device Name
- NV PRO3 MICRO BASE CHARGER
- Database Sync Date
- 2026-08-09 09:03:46
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 NVPRO3?
The registered manufacturer of record for NVPRO3 is DEN-MAT HOLDINGS, LLC.
What is the Primary UDI-DI identifier for NVPRO3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZLR3006.
What classification code is assigned to this device?
This device is registered under product classification code GEX.
Similar Classification Devices (GEX)
Other Devices by DEN-MAT HOLDINGS, LLC
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