gudid
Primary ID: 7753
PremierPro (UDI 7753)
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 7753
Device Regulatory Overview
The PremierPro (Model/Catalog Number: 7753) is a medical device manufactured by PRESTIGE AMERITECH, LTD.. This product is indexed under FDA Product Code / Category Classification IPR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7753
- Product Code / EMDN
- IPR
- Device Name
- Crutches, Bariatric, Adult, pairCrutch Height 47" - 55"Patient Height 5'2" - 5'10"
- Database Sync Date
- 2026-08-09 09:32:53
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 7753.
What classification code is assigned to this device?
This device is registered under product classification code IPR.
Similar Classification Devices (IPR)
Other Devices by PRESTIGE AMERITECH, LTD.
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