gudid
Primary ID: 8191
PremierPro (UDI 8191)
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 8191
Device Regulatory Overview
The PremierPro (Model/Catalog Number: 8191) is a medical device manufactured by PRESTIGE AMERITECH, LTD.. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8191
- Product Code / EMDN
- FQM
- Device Name
- CHOICE Cohesive Bandage, Non-Sterile, 1.5" Blue, 1.5"x5yards Stretched, Not made with Natural Rubber Latex
- Database Sync Date
- 2026-08-09 09:22:15
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 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 8191.
What classification code is assigned to this device?
This device is registered under product classification code FQM.
Similar Classification Devices (FQM)
Other Devices by PRESTIGE AMERITECH, LTD.
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