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basixCOMPAK™

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
basixCOMPAK™ FDA UDI
Generic Name
Catheter/overtube balloon inflator, single-use FDA UDI
Model / Reference
00884450021804 FDA UDI

Identifiers

Catalog Number
K05-00808 FDA UDI
Primary DI / UDI-DI
00884450021804 FDA UDI
FDA Product Code
OEQ FDA UDI
GMDN Term
Catheter/overtube balloon inflator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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: Catheter/overtube balloon inflator, single-use

The basixCOMPAK device is a comprehensive medical device designed to inflate and regulate the pressure of balloons used in various medical procedures. It features a dedicated manual syringe/plunger or electronic mechanism for inflation/deflation, an analogue/digital gauge/screen for monitoring pressure, and a locking mechanism.

Similar devices

Also classified as Catheter/overtube balloon inflator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 6bb542e5-a7cb-4b05-93ad-eebd8999947a 33 fields · synced Oct 6, 2026