gudid
Primary ID: ACC-HLD-100
Aqueduct SED (UDI ACC-HLD-100)
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-HLD-100
Device Regulatory Overview
The Aqueduct SED (Model/Catalog Number: ACC-HLD-100) 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-HLD-100
- Product Code / EMDN
- JXG
- Device Name
- The Aqueduct SED Drain Bag Holder interfaces with the Aqueduct SED Drain Bag (ACCBAG000) when in use with the Aqueduct SED Console (ACCCON101).
- 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-HLD-100.
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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