gudid
Primary ID: 42-2060
Curve (UDI 42-2060)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Curve - Primary ID 42-2060
Device Regulatory Overview
The Curve (Model/Catalog Number: 42-2060) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification KPM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42-2060
- Product Code / EMDN
- KPM
- Device Name
- Curve Ascites Shunt PAK, Ascites Shunt Percutaneous Access Kit / Double-Valved - 15.5 Fr
- 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 Curve?
The registered manufacturer of record for Curve is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for Curve?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42-2060.
What classification code is assigned to this device?
This device is registered under product classification code KPM.
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