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Tri-Flow

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
Tri-Flow FDA UDI
Generic Name
Double-lumen haemodialysis catheter, nonimplantable FDA UDI
Device Name
11.5F X 24CM Tri-Flow TRIPLE LUMEN CATHETER FULL TRAY FDA UDI
Model / Reference
MCDLT3-4424 FDA UDI
Description
11.5F X 24CM Tri-Flow TRIPLE LUMEN CATHETER FULL TRAY FDA UDI

Identifiers

Catalog Number
MCDLT3-4424 FDA UDI
Primary DI / UDI-DI
00884908175387 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Double-lumen haemodialysis catheter, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Double-lumen haemodialysis catheter, nonimplantable

Tri-Flow by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Double-lumen haemodialysis catheter, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Components Inc

Sources (1)

  • FDA UDI 381614aa-786b-484b-892c-7b6ec4e789ba 35 fields · synced Jun 8, 2026