← Back to catalogue

PowerPICC Provena

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
PowerPICC Provena FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
4 Fr Dual Lumen FDA UDI
Model / Reference
S3274155 FDA UDI
Description
4 Fr Dual Lumen FDA UDI

Identifiers

Catalog Number
S3274155 FDA UDI
Primary DI / UDI-DI
00801741130038 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Peripherally-inserted central venous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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

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
Catheter Gauge — 4 French FDA UDI
Length — 55 Centimeter FDA UDI

Category: Peripherally-inserted central venous catheter

A comprehensive device directory entry for the PowerPICC Provena medical device.

Similar devices

Also classified as Peripherally-inserted central venous catheter.

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 cad2efea-a803-4fe4-afe8-8aa349798194 36 fields · synced Jul 24, 2026