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Trio-Ct®

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
TRIO-CT® FDA UDI
Generic Name
Triple-lumen haemodialysis catheter FDA UDI
Device Name
13.5F X 30CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY FDA UDI
Model / Reference
ANG01135303 FDA UDI
Description
13.5F X 30CM TRIO-CT® TRIPLE LUMEN CATHETER MAX BARRIER PROCEDURE TRAY FDA UDI

Identifiers

Catalog Number
ANG01135303 FDA UDI
Primary DI / UDI-DI
00884908168259 FDA UDI
FDA Product Code
NIE FDA UDI
GMDN Term
Triple-lumen haemodialysis catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5540 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

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: Triple-lumen haemodialysis catheter

Trio-Ct® by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Triple-lumen haemodialysis catheter.

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 05355a19-b61a-4b74-bbf9-4b760d976b97 35 fields · synced May 30, 2026