gudid
Primary ID: RecoveryPulse Arm EXTRA LARGE
Therabody (UDI RecoveryPulse Arm EXTRA LARGE)
Manufactured by Therabody, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Therabody - Primary ID RecoveryPulse Arm EXTRA LARGE
Device Regulatory Overview
The Therabody (Model/Catalog Number: RecoveryPulse Arm EXTRA LARGE) is a medical device manufactured by Therabody, Inc.. This product is indexed under FDA Product Code / Category Classification ISA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RecoveryPulse Arm EXTRA LARGE
- Product Code / EMDN
- ISA
- Device Name
- Database Sync Date
- 2026-08-09 09:17:03
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 Therabody?
The registered manufacturer of record for Therabody is Therabody, Inc..
What is the Primary UDI-DI identifier for Therabody?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RecoveryPulse Arm EXTRA LARGE.
What classification code is assigned to this device?
This device is registered under product classification code ISA.
Similar Classification Devices (ISA)
Other Devices by Therabody, Inc.
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