gudid
Primary ID: D5061
PremierPro (UDI D5061)
Manufactured by PRESTIGE AMERITECH, LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PremierPro - Primary ID D5061
Device Regulatory Overview
The PremierPro (Model/Catalog Number: D5061) is a medical device manufactured by PRESTIGE AMERITECH, LTD.. This product is indexed under FDA Product Code / Category Classification LZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D5061
- Product Code / EMDN
- LZC
- Device Name
- PremierPro Plus Powered by Honeywell Nitrile Exam Glove XSmall 200count
- Database Sync Date
- 2026-08-09 09:22:15
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PremierPro?
The registered manufacturer of record for PremierPro is PRESTIGE AMERITECH, LTD..
What is the Primary UDI-DI identifier for PremierPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D5061.
What classification code is assigned to this device?
This device is registered under product classification code LZC.
Similar Classification Devices (LZC)
Other Devices by PRESTIGE AMERITECH, LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint