Merit Medical®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name: Merit Medical® FDA UDI
Generic Name: Radiographic procedure tubing FDA UDI
Model / Reference: 00884450029886 FDA UDI

Identifiers

Catalog Number: HP9200E FDA UDI
Primary DI / UDI-DI: 00884450029886 FDA UDI
FDA Product Code: DXJ FDA UDI
GMDN Term: Radiographic procedure tubing FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2450 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Radiographic procedure tubing

Merit Medical's Radiographic Procedure Tubing is a flexible, cylindrical device designed to connect a contrast imaging syringe to a patient cannula for diagnostic radiographic procedures. This device features low and high pressure capabilities, accommodating various lengths with quick connecting fittings. It is sterilized using autoclaving and has an expiration date. The product is provided in one base package and has been manufactured since 2021.

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Also classified as Radiographic procedure tubing.

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10” (25 cm) High Pressure Connector Tube — Bayer Medical Care Inc. · Class II

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: Merit Medical Systems, Inc.

Sources (1)

FDA UDI c05e5a94-8856-4744-88c9-004bc92c94c9 34 fields · synced Oct 6, 2026