gudid
Primary ID: ZLR3003INT
NV PRO3 (UDI ZLR3003INT)
Manufactured by DEN-MAT HOLDINGS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NV PRO3 - Primary ID ZLR3003INT
Device Regulatory Overview
The NV PRO3 (Model/Catalog Number: ZLR3003INT) 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
- ZLR3003INT
- Product Code / EMDN
- GEX
- Device Name
- NV PRO3 MICROLASER IT
- 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 NV PRO3?
The registered manufacturer of record for NV PRO3 is DEN-MAT HOLDINGS, LLC.
What is the Primary UDI-DI identifier for NV PRO3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZLR3003INT.
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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