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Arrow

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
ARROW(R) PICC powered by ARROW(R) VPS TipTracker(TM) Stylet FDA UDI
Model / Reference
IPN037876 FDA UDI
Description
ARROW(R) PICC powered by ARROW(R) VPS TipTracker(TM) Stylet FDA UDI

Identifiers

Catalog Number
CDC-45541-TTS FDA UDI
Primary DI / UDI-DI
30801902132865 FDA UDI
510(k) Number
K160925 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

Category: Peripherally-inserted central venous catheter

Arrow by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 422b1fb4-2a11-4c6a-beb7-a604ed1a9283 37 fields · synced May 30, 2026