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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
Contrast medium injection system administration set FDA UDI
Model / Reference
00884450210291 FDA UDI

Identifiers

Primary DI / UDI-DI
00884450210291 FDA UDI
FDA Product Code
OEZ FDA UDI
GMDN Term
Contrast medium injection system administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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: Contrast medium injection system administration set

Merit Medical's Cardiovascular Procedure Kit is a disposable contrast medium injection system administration set designed for implantable devices. With its unique design and features, this kit provides reliable and efficient fluid delivery during medical procedures.

Similar devices

Also classified as Contrast medium injection system administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 240f9ec7-2ca6-4836-96a6-c1c6babe5fbf 32 fields · synced Jul 10, 2026