gudid
Primary ID: 1068503
PureOrtho (UDI 1068503)
Manufactured by PURELIFE, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PureOrtho - Primary ID 1068503
Device Regulatory Overview
The PureOrtho (Model/Catalog Number: 1068503) is a medical device manufactured by PURELIFE, LLC. This product is indexed under FDA Product Code / Category Classification LZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1068503
- Product Code / EMDN
- LZC
- Device Name
- PureOrtho Nitrile Powder-Free, Medium, Nitrile powder-free gloves, Tiffany blue in color, Packaging contains recycled material
- Database Sync Date
- 2026-08-09 09:05:50
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 PureOrtho?
The registered manufacturer of record for PureOrtho is PURELIFE, LLC.
What is the Primary UDI-DI identifier for PureOrtho?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1068503.
What classification code is assigned to this device?
This device is registered under product classification code LZC.
Similar Classification Devices (LZC)
Other Devices by PURELIFE, LLC
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