KFBIO (UDI 06975330712142)
Manufactured by NINGBO KONFOONG BIOINFORMATION TECH CO., LTD.
Device Regulatory Overview
The KFBIO (Model/Catalog Number: 2142) is a medical device manufactured by NINGBO KONFOONG BIOINFORMATION TECH CO., LTD.. This product is indexed under FDA Product Code / Category Classification W02069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2142
- Product Code / EMDN
- W02069099
- Device Name
- Stainer and Coverslipper
- Database Sync Date
- 2026-08-09 16:47:59
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 KFBIO?
The registered manufacturer of record for KFBIO is NINGBO KONFOONG BIOINFORMATION TECH CO., LTD..
What is the Primary UDI-DI identifier for KFBIO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975330712142.
What classification code is assigned to this device?
This device is registered under product classification code W02069099.
Similar Classification Devices (W02069099)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint