patient monitor (UDI 06932562300813)
Manufactured by Guangdong Biolight Meditech Co., Ltd
Device Regulatory Overview
The patient monitor (Model/Catalog Number: Truscope P1) is a medical device manufactured by Guangdong Biolight Meditech Co., Ltd. This product is indexed under FDA Product Code / Category Classification Z1203020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Truscope P1
- Product Code / EMDN
- Z1203020201
- Device Name
- patient monitor
- Database Sync Date
- 2026-08-09 16:29:16
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 patient monitor?
The registered manufacturer of record for patient monitor is Guangdong Biolight Meditech Co., Ltd.
What is the Primary UDI-DI identifier for patient monitor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06932562300813.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020201.
Similar Classification Devices (Z1203020201)
Other Devices by Guangdong Biolight Meditech Co., Ltd
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