gudid
Primary ID: SW305
Aurora Hydrocolloide Adhesive Sheath (UDI SW305)
Manufactured by C. R. Bard, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aurora Hydrocolloide Adhesive Sheath - Primary ID SW305
Device Regulatory Overview
The Aurora Hydrocolloide Adhesive Sheath (Model/Catalog Number: SW305) is a medical device manufactured by C. R. Bard, Inc.. This product is indexed under FDA Product Code / Category Classification NNX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SW305
- Product Code / EMDN
- NNX
- Device Name
- Aurora Condomcatheter Met Hydrocolloide Kleefzone
- Database Sync Date
- 2026-08-09 09:52:56
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 Aurora Hydrocolloide Adhesive Sheath?
The registered manufacturer of record for Aurora Hydrocolloide Adhesive Sheath is C. R. Bard, Inc..
What is the Primary UDI-DI identifier for Aurora Hydrocolloide Adhesive Sheath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SW305.
What classification code is assigned to this device?
This device is registered under product classification code NNX.
Similar Classification Devices (NNX)
Other Devices by C. R. Bard, Inc.
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