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