SITE-SCRUB (UDI 3882100)
Manufactured by Bard Access Systems, Inc.
Device Regulatory Overview
The SITE-SCRUB (Model/Catalog Number: 3882100) is a medical device manufactured by Bard Access Systems, Inc.. This product is indexed under FDA Product Code / Category Classification LKB 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
- 3882100
- Product Code / EMDN
- LKB
- Device Name
- Site-ScrubTM IPA Device
- Database Sync Date
- 2026-08-09 10:00:15
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 SITE-SCRUB?
The registered manufacturer of record for SITE-SCRUB is Bard Access Systems, Inc..
What is the Primary UDI-DI identifier for SITE-SCRUB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3882100.
What classification code is assigned to this device?
This device is registered under product classification code LKB.
Similar Classification Devices (LKB)
Other Devices by Bard Access Systems, Inc.
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