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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, non-medicated FDA UDI
Device Name
UNIVERSAL BLOCK TRAY FDA UDI
Model / Reference
34-8317A FDA UDI
Description
UNIVERSAL BLOCK TRAY FDA UDI

Identifiers

Catalog Number
34-8317A FDA UDI
Primary DI / UDI-DI
10888439666793 FDA UDI
FDA Product Code
OGJ FDA UDI
GMDN Term
Peripheral anaesthesia single-administration set, non-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, non-medicated

Cardinal Health Universal Block Tray is a single-administration peripheral nerve-block set for anaesthesia. This device is designed as a collection of devices intended for the single-administration of an anaesthetic agent, not including a catheter. It includes an anaesthesia needle and a syringe with additional devices for the procedure. The tray can be used for dental applications but is also marketed for use in various fields.

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b289550-332c-4475-8206-316beaaae638 35 fields · synced Jul 15, 2026