gudid
Primary ID: ACC-KIT-101
Aqueduct SED (UDI ACC-KIT-101)
Manufactured by AQUEDUCT CRITICAL CARE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aqueduct SED - Primary ID ACC-KIT-101
Device Regulatory Overview
The Aqueduct SED (Model/Catalog Number: ACC-KIT-101) is a medical device manufactured by AQUEDUCT CRITICAL CARE, INC.. This product is indexed under FDA Product Code / Category Classification JXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACC-KIT-101
- Product Code / EMDN
- JXG
- Device Name
- The Aqueduct Smart External Drain Kit is a convenience kit of the re-usable portions of the Aqueduct SED System. The Aqueduct SED system is a collection of devices for Monitoring of intracranial pressure (ICP) and draining and monitoring of CSF flow from the lateral ventricles.This kit contains ACCCON101 and ACCHLD100.
- Database Sync Date
- 2026-08-09 09:16:45
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 Aqueduct SED?
The registered manufacturer of record for Aqueduct SED is AQUEDUCT CRITICAL CARE, INC..
What is the Primary UDI-DI identifier for Aqueduct SED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACC-KIT-101.
What classification code is assigned to this device?
This device is registered under product classification code JXG.
Similar Classification Devices (JXG)
Other Devices by AQUEDUCT CRITICAL CARE, INC.
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