SpO2 sensor (UDI 06932562300677)
Manufactured by Guangdong Biolight Meditech Co., Ltd
Device Regulatory Overview
The SpO2 sensor (Model/Catalog Number: SRA-P12/15-100-0323) is a medical device manufactured by Guangdong Biolight Meditech Co., Ltd. This product is indexed under FDA Product Code / Category Classification Z1203020285 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SRA-P12/15-100-0323
- Product Code / EMDN
- Z1203020285
- Device Name
- SpO2 sensor
- Database Sync Date
- 2026-08-09 17:25:29
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 SpO2 sensor?
The registered manufacturer of record for SpO2 sensor is Guangdong Biolight Meditech Co., Ltd.
What is the Primary UDI-DI identifier for SpO2 sensor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06932562300677.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020285.
Similar Classification Devices (Z1203020285)
Other Devices by Guangdong Biolight Meditech Co., Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint