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Curity

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Lumbar puncture kit FDA UDI
Device Name
Infant Lumbar Puncture Tray with Safety Components FDA UDI
Model / Reference
7039 FDA UDI
Description
Infant Lumbar Puncture Tray with Safety Components FDA UDI

Identifiers

Catalog Number
7039 FDA UDI
Primary DI / UDI-DI
10884521020399 FDA UDI
FDA Product Code
PWY FDA UDI
GMDN Term
Lumbar puncture kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

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: Lumbar puncture kit

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

Similar devices

Also classified as Lumbar puncture kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI afcb408b-0520-4be4-a3bd-eac946630df8 35 fields · synced May 31, 2026