Allegro Nextgen Reformer™ Tower & Mat Conversion (UDI 00810052141879)
Manufactured by Balanced Body Inc
Device Regulatory Overview
The Allegro Nextgen Reformer™ Tower & Mat Conversion (Model/Catalog Number: 19057C) is a medical device manufactured by Balanced Body Inc. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19057C
- Product Code / EMDN
- Z12069099
- Device Name
- Reformer-Trapeze Combination (RTC)
- Database Sync Date
- 2026-08-09 16:28:44
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 Allegro Nextgen Reformer™ Tower & Mat Conversion?
The registered manufacturer of record for Allegro Nextgen Reformer™ Tower & Mat Conversion is Balanced Body Inc.
What is the Primary UDI-DI identifier for Allegro Nextgen Reformer™ Tower & Mat Conversion?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810052141879.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
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