gudid
Primary ID: PAS-02
Passio Redressing Kit (UDI PAS-02)
Manufactured by Bearpac Medical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Passio Redressing Kit - Primary ID PAS-02
Device Regulatory Overview
The Passio Redressing Kit (Model/Catalog Number: PAS-02) is a medical device manufactured by Bearpac Medical, LLC. This product is indexed under FDA Product Code / Category Classification DWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PAS-02
- Product Code / EMDN
- DWM
- Device Name
- Database Sync Date
- 2026-08-09 09:08:43
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 Passio Redressing Kit?
The registered manufacturer of record for Passio Redressing Kit is Bearpac Medical, LLC.
What is the Primary UDI-DI identifier for Passio Redressing Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PAS-02.
What classification code is assigned to this device?
This device is registered under product classification code DWM.
Similar Classification Devices (DWM)
Other Devices by Bearpac Medical, LLC
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