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Curity

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Aspiration tray, single-use FDA UDI
Device Name
Thoracentesis Tray with Safety Components FDA UDI
Model / Reference
5016 FDA UDI
Description
Thoracentesis Tray with Safety Components FDA UDI

Identifiers

Catalog Number
5016 FDA UDI
Primary DI / UDI-DI
10884521020382 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Aspiration tray, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Aspiration tray, single-use

Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aspiration tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI a11ba7bb-ade6-4b5b-95d7-e92ff2d51eb5 36 fields · synced Jun 1, 2026