← Back to catalogue

Brevia Short Term Dialysis Catheter

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Brevia Short Term Dialysis Catheter FDA UDI
Generic Name
Double-lumen haemodialysis catheter, implantable FDA UDI
Device Name
DOT, Brevia Catheter FDA UDI
Model / Reference
5565200 FDA UDI
Description
DOT, Brevia Catheter FDA UDI

Identifiers

Catalog Number
5565200 FDA UDI
Primary DI / UDI-DI
00801741045479 FDA UDI
FDA Product Code
LFJ FDA UDI
GMDN Term
Double-lumen haemodialysis catheter, implantable 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

Yes

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

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI
Catheter Gauge — 11 French FDA UDI

Category: Double-lumen haemodialysis catheter, implantable

Brevia Short Term Dialysis Catheter by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Double-lumen haemodialysis catheter, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI e3ffed0e-e2f2-40c5-8a09-121ae7556b69 37 fields · synced Jun 9, 2026