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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 / Double-Valved - 11.5 Fr FDA UDI
Model / Reference
42-2070 FDA UDI
Description
Curve Ascites Shunt PAK, Ascites Shunt Percutaneous Access Kit / Double-Valved - 11.5 Fr FDA UDI

Identifiers

Catalog Number
42-2070 FDA UDI
Primary DI / UDI-DI
10885403241208 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

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Manufacturer

Manufacturer
Carefusion 2200, Inc.

Sources (1)

  • FDA UDI 973bc440-c76c-4c0c-ac09-06166b8a6bd3 35 fields · synced Sep 18, 2026