gudid
Primary ID: C86053
iFlash-hGH (UDI C86053)
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-hGH - Primary ID C86053
Device Regulatory Overview
The iFlash-hGH (Model/Catalog Number: C86053) is a medical device manufactured by Shenzhen YHLO Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification CFL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C86053
- Product Code / EMDN
- CFL
- Device Name
- Database Sync Date
- 2026-08-09 09:24:52
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of iFlash-hGH?
The registered manufacturer of record for iFlash-hGH is Shenzhen YHLO Biotech Co., Ltd..
What is the Primary UDI-DI identifier for iFlash-hGH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C86053.
What classification code is assigned to this device?
This device is registered under product classification code CFL.
Similar Classification Devices (CFL)
Other Devices by Shenzhen YHLO Biotech Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint