eudamed_udi
Primary ID: 00810052140391
Clinical Reformer® with Tower and Mat (UDI 00810052140391)
Manufactured by Balanced Body Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Clinical Reformer® with Tower and Mat - Primary ID 00810052140391
Device Regulatory Overview
The Clinical Reformer® with Tower and Mat (Model/Catalog Number: 12251) 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
- 12251
- Product Code / EMDN
- Z12069099
- Device Name
- Reformer-Trapeze Combination (RTC)
- Database Sync Date
- 2026-08-09 16:29:35
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 Clinical Reformer® with Tower and Mat?
The registered manufacturer of record for Clinical Reformer® with Tower and Mat is Balanced Body Inc.
What is the Primary UDI-DI identifier for Clinical Reformer® with Tower and Mat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810052140391.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint