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Leader

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 110, Inc.

Identity

Trade Name
LEADER FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
LDR Nebulizer System All-in-One 1 count FDA UDI
Model / Reference
5966312 FDA UDI
Description
LDR Nebulizer System All-in-One 1 count FDA UDI

Identifiers

Catalog Number
5966312 FDA UDI
Primary DI / UDI-DI
00096295145106 FDA UDI
510(k) Number
K043238 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nebulizing system delivery set, reusable

Leader by Cardinal Health 110, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e22fb450-29ac-4195-bc5c-7986a0268609 37 fields · synced Jun 8, 2026