Grandeur Series Lightweight Adult Dual Head Stethoscope (UDI 04719890206268)
Manufactured by CHIN KOU MEDICAL INSTRUMENT CO., LTD.
Device Regulatory Overview
The Grandeur Series Lightweight Adult Dual Head Stethoscope (Model/Catalog Number: CK-A601GDPF) is a medical device manufactured by CHIN KOU MEDICAL INSTRUMENT CO., LTD.. This product is indexed under FDA Product Code / Category Classification C9005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CK-A601GDPF
- Product Code / EMDN
- C9005
- Device Name
- Regalite Single Head Stethoscope
- Database Sync Date
- 2026-08-09 16:28:48
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 Grandeur Series Lightweight Adult Dual Head Stethoscope?
The registered manufacturer of record for Grandeur Series Lightweight Adult Dual Head Stethoscope is CHIN KOU MEDICAL INSTRUMENT CO., LTD..
What is the Primary UDI-DI identifier for Grandeur Series Lightweight Adult Dual Head Stethoscope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719890206268.
What classification code is assigned to this device?
This device is registered under product classification code C9005.
Similar Classification Devices (C9005)
Other Devices by CHIN KOU MEDICAL INSTRUMENT CO., LTD.
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