gudid
Primary ID: PW300CASE
PureWick (UDI PW300CASE)
Manufactured by C. R. Bard, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PureWick - Primary ID PW300CASE
Device Regulatory Overview
The PureWick (Model/Catalog Number: PW300CASE) is a medical device manufactured by C. R. Bard, Inc.. This product is indexed under FDA Product Code / Category Classification NZU within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PW300CASE
- Product Code / EMDN
- NZU
- Device Name
- PureWick Urine Collection System
- Database Sync Date
- 2026-08-09 09:52:54
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 PureWick?
The registered manufacturer of record for PureWick is C. R. Bard, Inc..
What is the Primary UDI-DI identifier for PureWick?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PW300CASE.
What classification code is assigned to this device?
This device is registered under product classification code NZU.
Similar Classification Devices (NZU)
Other Devices by C. R. Bard, Inc.
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