gudid
Primary ID: 52822-220
VersaTREK (UDI 52822-220)
Manufactured by REMEL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VersaTREK - Primary ID 52822-220
Device Regulatory Overview
The VersaTREK (Model/Catalog Number: 52822-220) is a medical device manufactured by REMEL, INC.. This product is indexed under FDA Product Code / Category Classification MDB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 52822-220
- Product Code / EMDN
- MDB
- Device Name
- Y52822220 VERSATREK 528 W/22 DR/CTRL MOD 220V
- Database Sync Date
- 2026-08-09 09:35:51
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 VersaTREK?
The registered manufacturer of record for VersaTREK is REMEL, INC..
What is the Primary UDI-DI identifier for VersaTREK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 52822-220.
What classification code is assigned to this device?
This device is registered under product classification code MDB.
Similar Classification Devices (MDB)
Other Devices by REMEL, INC.
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