Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: CARDINAL HEALTH FDA UDI
Generic Name: Epidural anaesthesia set, non-medicated FDA UDI
Device Name: STERILE EPIDURAL TRAY FDA UDI
Model / Reference: 13-2300A FDA UDI
Description: STERILE EPIDURAL TRAY FDA UDI

Identifiers

Catalog Number: 13-2300A FDA UDI
Primary DI / UDI-DI: 10887488319865 FDA UDI
FDA Product Code: OGE FDA UDI
GMDN Term: Epidural anaesthesia set, non-medicated FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5120 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Epidural anaesthesia set, non-medicated

Cardinal Health by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cardinal Health 200, LLC

Sources (1)

FDA UDI 95ca64e7-7cb4-47cb-831a-83f64930136c 35 fields · synced Jun 8, 2026