eudamed_udi
Primary ID: 17540176030192
ReGrasp Clinician Pro 2 (UDI 17540176030192)
Manufactured by Rehabtronics
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReGrasp Clinician Pro 2 - Primary ID 17540176030192
Device Regulatory Overview
The ReGrasp Clinician Pro 2 (Model/Catalog Number: EPKTS) is a medical device manufactured by Rehabtronics. This product is indexed under FDA Product Code / Category Classification Z12062880 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EPKTS
- Product Code / EMDN
- Z12062880
- Device Name
- Electronic Positioning Kit Version 2
- Database Sync Date
- 2026-08-09 16:29:04
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 ReGrasp Clinician Pro 2?
The registered manufacturer of record for ReGrasp Clinician Pro 2 is Rehabtronics.
What is the Primary UDI-DI identifier for ReGrasp Clinician Pro 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 17540176030192.
What classification code is assigned to this device?
This device is registered under product classification code Z12062880.
Similar Classification Devices (Z12062880)
Other Devices by Rehabtronics
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