gudid
Primary ID: C89948
Trigger Solution (1) (UDI C89948)
Manufactured by Shenzhen YHLO Biotech Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trigger Solution (1) - Primary ID C89948
Device Regulatory Overview
The Trigger Solution (1) (Model/Catalog Number: C89948) is a medical device manufactured by Shenzhen YHLO Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PPM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C89948
- Product Code / EMDN
- PPM
- Device Name
- 220 mL4 bottles
- Database Sync Date
- 2026-08-09 09:24:52
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 Trigger Solution (1)?
The registered manufacturer of record for Trigger Solution (1) is Shenzhen YHLO Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Trigger Solution (1)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C89948.
What classification code is assigned to this device?
This device is registered under product classification code PPM.
Similar Classification Devices (PPM)
Other Devices by Shenzhen YHLO Biotech Co., Ltd.
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