gudid
Primary ID: AST-905B
Creliver (UDI AST-905B)
Manufactured by Shenzhen Osto Technology Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Creliver - Primary ID AST-905B
Device Regulatory Overview
The Creliver (Model/Catalog Number: AST-905B) is a medical device manufactured by Shenzhen Osto Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification NGX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AST-905B
- Product Code / EMDN
- NGX
- Device Name
- Database Sync Date
- 2026-08-09 09:05:25
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 Creliver?
The registered manufacturer of record for Creliver is Shenzhen Osto Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Creliver?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AST-905B.
What classification code is assigned to this device?
This device is registered under product classification code NGX.
Similar Classification Devices (NGX)
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