Blood Glucose Meter (UDI 06950715500484)
Manufactured by Cofoe Medical Technology Co.,Ltd.
Device Regulatory Overview
The Blood Glucose Meter (Model/Catalog Number: KFA103) is a medical device manufactured by Cofoe Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0201060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KFA103
- Product Code / EMDN
- W0201060102
- Device Name
- Blood Glucose Meter
- Database Sync Date
- 2026-08-09 18:07:34
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 Blood Glucose Meter?
The registered manufacturer of record for Blood Glucose Meter is Cofoe Medical Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Blood Glucose Meter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06950715500484.
What classification code is assigned to this device?
This device is registered under product classification code W0201060102.
Similar Classification Devices (W0201060102)
Other Devices by Cofoe Medical Technology Co.,Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint