itool ApexPulse (UDI 201-00-50)
Manufactured by Apex (Guangzhou) Tools & Orthopedics Co.
Device Regulatory Overview
The itool ApexPulse (Model/Catalog Number: 201-00-50) is a medical device manufactured by Apex (Guangzhou) Tools & Orthopedics Co.. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201-00-50
- Product Code / EMDN
- FQH
- Device Name
- SHOWER SPRAY TIP
- Database Sync Date
- 2026-08-09 09:05:24
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 itool ApexPulse?
The registered manufacturer of record for itool ApexPulse is Apex (Guangzhou) Tools & Orthopedics Co..
What is the Primary UDI-DI identifier for itool ApexPulse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 201-00-50.
What classification code is assigned to this device?
This device is registered under product classification code FQH.
Similar Classification Devices (FQH)
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