← Back to catalogue

Curve

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
Curve FDA UDI
Generic Name
Interventional radiology percutaneous-access kit, single-use FDA UDI
Device Name
Curve Ascites Shunt PAK, Ascites Shunt Percutaneous Access Kit / Single-Valved - 15.5 Fr FDA UDI
Model / Reference
42-2065 FDA UDI
Description
Curve Ascites Shunt PAK, Ascites Shunt Percutaneous Access Kit / Single-Valved - 15.5 Fr FDA UDI

Identifiers

Catalog Number
42-2065 FDA UDI
Primary DI / UDI-DI
10885403471230 FDA UDI
FDA Product Code
DYB FDA UDI
KPM FDA UDI
GMDN Term
Interventional radiology percutaneous-access kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 FDA UDI
876.5955 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Interventional radiology percutaneous-access kit, single-use

Curve by Carefusion 2200, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interventional radiology percutaneous-access kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Carefusion 2200, Inc.

Sources (1)

  • FDA UDI ef8fd3ee-9f57-4279-a3b4-827a1049c241 35 fields · synced Sep 18, 2026