2.30MHZ PRECORDIAL PROBE (UDI 832-5230-12)
Manufactured by PARKS MEDICAL ELECTRONICS, INC.
Device Regulatory Overview
The 2.30MHZ PRECORDIAL PROBE (Model/Catalog Number: 832-5230-12) is a medical device manufactured by PARKS MEDICAL ELECTRONICS, INC.. This product is indexed under FDA Product Code / Category Classification JOP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 832-5230-12
- Product Code / EMDN
- JOP
- Device Name
- Database Sync Date
- 2026-08-09 09:31:28
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 2.30MHZ PRECORDIAL PROBE?
The registered manufacturer of record for 2.30MHZ PRECORDIAL PROBE is PARKS MEDICAL ELECTRONICS, INC..
What is the Primary UDI-DI identifier for 2.30MHZ PRECORDIAL PROBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 832-5230-12.
What classification code is assigned to this device?
This device is registered under product classification code JOP.
Similar Classification Devices (JOP)
Other Devices by PARKS MEDICAL ELECTRONICS, INC.
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