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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
Cervical anaesthesia kit FDA UDI
Device Name
PAIN TRAY FDA UDI
Model / Reference
13-6814B FDA UDI
Description
PAIN TRAY FDA UDI

Identifiers

Catalog Number
13-6814B FDA UDI
Primary DI / UDI-DI
10888439037906 FDA UDI
FDA Product Code
OFQ FDA UDI
GMDN Term
Cervical anaesthesia kit 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

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: Cervical anaesthesia kit

The Cervical Anaesthesia Kit from Cardinal Health is a sterile device designed to deliver an analgesic or anaesthetic agent for use in various medical procedures, including gynecological diagnostic tests and pain management during labor and delivery. This single-use kit consists of a procedural needle, syringe, catheter, and filter, and is typically used in conjunction with other devices such as the Cervical Needle Guide Tube (CNGT).

Similar devices

Also classified as Cervical anaesthesia kit.

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 d80f0e07-7ab4-4cbb-8412-aed3e9be6e0b 35 fields · synced Jul 21, 2026