← Back to catalogue

Merit Medical®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Merit Medical® FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Model / Reference
00884450250389 FDA UDI

Identifiers

Catalog Number
K08-02939A FDA UDI
Primary DI / UDI-DI
00884450250389 FDA UDI
FDA Product Code
OJA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive 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

No

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: Basic intravenous administration set, noninvasive

A comprehensive intravenous administration set designed for single-use, noninvasive use in medical settings. The Merit Medical Intravenous Extension Tubing Set is a valuable tool for healthcare professionals, providing easy access to fluids and nutrients.

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b1d3f0a9-9efb-4aee-b877-70a9b355e186 33 fields · synced Jul 25, 2026