gudid
Primary ID: CFR2220
N/A (UDI CFR2220)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID CFR2220
Device Regulatory Overview
The N/A (Model/Catalog Number: CFR2220) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CFR2220
- Product Code / EMDN
- KNW
- Device Name
- Coaxial Franseen Fine Needle Aspiration, 22 G x 20 cm
- Database Sync Date
- 2026-08-09 09:16:32
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 N/A?
The registered manufacturer of record for N/A is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CFR2220.
What classification code is assigned to this device?
This device is registered under product classification code KNW.
Similar Classification Devices (KNW)
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