Provena (UDI CK001092A)
Manufactured by Bard Access Systems, Inc.
Device Regulatory Overview
The Provena (Model/Catalog Number: CK001092A) is a medical device manufactured by Bard Access Systems, Inc.. This product is indexed under FDA Product Code / Category Classification PND within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- CK001092A
- Product Code / EMDN
- PND
- Device Name
- Catheter Placement kit
- 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 Provena?
The registered manufacturer of record for Provena is Bard Access Systems, Inc..
What is the Primary UDI-DI identifier for Provena?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CK001092A.
What classification code is assigned to this device?
This device is registered under product classification code PND.
Similar Classification Devices (PND)
Other Devices by Bard Access Systems, Inc.
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