gudid
Primary ID: C88004M
iFlash-Mycoplasma pn. IgM (UDI C88004M)
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 iFlash-Mycoplasma pn. IgM - Primary ID C88004M
Device Regulatory Overview
The iFlash-Mycoplasma pn. IgM (Model/Catalog Number: C88004M) is a medical device manufactured by Shenzhen YHLO Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification GSA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C88004M
- Product Code / EMDN
- GSA
- Device Name
- 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 iFlash-Mycoplasma pn. IgM?
The registered manufacturer of record for iFlash-Mycoplasma pn. IgM is Shenzhen YHLO Biotech Co., Ltd..
What is the Primary UDI-DI identifier for iFlash-Mycoplasma pn. IgM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C88004M.
What classification code is assigned to this device?
This device is registered under product classification code GSA.
Similar Classification Devices (GSA)
Other Devices by Shenzhen YHLO Biotech Co., Ltd.
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