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Power-Trialysis Slim-Cath catheter

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Power-Trialysis Slim-Cath catheter FDA UDI
Generic Name
Triple-lumen haemodialysis catheter FDA UDI
Device Name
12Fr Trialysis PC 15cm Kit FDA UDI
Model / Reference
5863150 FDA UDI
Description
12Fr Trialysis PC 15cm Kit FDA UDI

Identifiers

Catalog Number
5863150 FDA UDI
Primary DI / UDI-DI
00801741107283 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

Dimensions & Sizes

Size
Length — 15 Centimeter FDA UDI
Catheter Gauge — 12 French FDA UDI

Category: Triple-lumen haemodialysis catheter

Power-Trialysis Slim-Cath catheter by Bard Access Systems, 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

Sources (1)

  • FDA UDI a24d54cc-067c-4654-8dca-d638f3fb40a0 36 fields · synced Jun 9, 2026