Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay) (UDI 06970341681517)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay) (Model/Catalog Number: 745001) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102069013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 745001
- Product Code / EMDN
- W0102069013
- Device Name
- Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay)
- Database Sync Date
- 2026-08-09 17:03:08
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 Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay)?
The registered manufacturer of record for Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay) is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Procalcitonin (PCT) Assay Kits (Lateral Flow Immunoassay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970341681517.
What classification code is assigned to this device?
This device is registered under product classification code W0102069013.
Similar Classification Devices (W0102069013)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
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