gudid
Primary ID: GAR048
AquaPulse (UDI GAR048)
Manufactured by Smartdata Suzhou Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AquaPulse - Primary ID GAR048
Device Regulatory Overview
The AquaPulse (Model/Catalog Number: GAR048) is a medical device manufactured by Smartdata Suzhou Co., Ltd.. This product is indexed under FDA Product Code / Category Classification OCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GAR048
- Product Code / EMDN
- OCX
- Device Name
- Auxiliary Water Connector
- Database Sync Date
- 2026-08-09 09:06:47
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 AquaPulse?
The registered manufacturer of record for AquaPulse is Smartdata Suzhou Co., Ltd..
What is the Primary UDI-DI identifier for AquaPulse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GAR048.
What classification code is assigned to this device?
This device is registered under product classification code OCX.
Similar Classification Devices (OCX)
Other Devices by Smartdata Suzhou Co., Ltd.
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