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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
00884450207895 FDA UDI

Identifiers

Primary DI / UDI-DI
00884450207895 FDA UDI
FDA Product Code
OJA FDA UDI
GMDN Term
Radiographic procedure tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

No

FDA UDI

Category: Radiographic procedure tubing

Merit Medical offers a flexible, portable radiographic procedure tubing solution for the safe and efficient transfer of contrast media and fluids during diagnostic imaging procedures. Our device is designed to accommodate various lengths with quick connecting fittings, making it an ideal choice for healthcare professionals.

Similar devices

Also classified as Radiographic procedure tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 325af799-35df-4c7c-a962-db2c0aa228d8 32 fields · synced Jul 18, 2026