PCT Fast Test Kit (Immunofluorescence Assay) (UDI 06954414702071)
Manufactured by Getein Biotech, Inc.
Device Regulatory Overview
The PCT Fast Test Kit (Immunofluorescence Assay) (Model/Catalog Number: /) is a medical device manufactured by Getein Biotech, Inc.. This product is indexed under FDA Product Code / Category Classification W0102069013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W0102069013
- Device Name
- PCT Fast Test Kit (Immunofluorescence Assay)
- Database Sync Date
- 2026-08-09 16:59:27
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 PCT Fast Test Kit (Immunofluorescence Assay)?
The registered manufacturer of record for PCT Fast Test Kit (Immunofluorescence Assay) is Getein Biotech, Inc..
What is the Primary UDI-DI identifier for PCT Fast Test Kit (Immunofluorescence Assay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414702071.
What classification code is assigned to this device?
This device is registered under product classification code W0102069013.
Similar Classification Devices (W0102069013)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint