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Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Peripheral anaesthesia single-administration set, medicated FDA UDI
Device Name
INTERVENTIONAL NERVE BLOCK KIT FDA UDI
Model / Reference
SBA73INNVK FDA UDI
Description
INTERVENTIONAL NERVE BLOCK KIT FDA UDI

Identifiers

Catalog Number
SBA73INNVK FDA UDI
Primary DI / UDI-DI
10888439826531 FDA UDI
FDA Product Code
OGJ FDA UDI
GMDN Term
Peripheral anaesthesia single-administration set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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

Yes

FDA UDI

Category: Peripheral anaesthesia single-administration set, medicated

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

Similar devices

Also classified as Peripheral anaesthesia single-administration set, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 786055fe-265e-487b-9283-c3fc72daddbc 35 fields · synced Jun 6, 2026