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FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
ARROWg+ard Blue(R) PSI Kit Cath-Gard(R) for use with 7.5 - 8 Fr. Catheters FDA UDI
Model / Reference
IPN035514 FDA UDI
Description
ARROWg+ard Blue(R) PSI Kit Cath-Gard(R) for use with 7.5 - 8 Fr. Catheters FDA UDI

Identifiers

Catalog Number
CDC-29903-1A FDA UDI
Primary DI / UDI-DI
10801902044829 FDA UDI
510(k) Number
K011761 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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

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

Category: Vascular catheter introduction set, nonimplantable

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

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

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 2c04de4f-a66e-4f11-9dc3-b1b1efee8b23 37 fields · synced Jun 8, 2026