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Arrow

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Peripheral artery cannula FDA UDI
Device Name
Radial Artery Catheterization Kit FDA UDI
Model / Reference
IPN037567 FDA UDI
Description
Radial Artery Catheterization Kit FDA UDI

Identifiers

Catalog Number
ASK-04020-HH1 FDA UDI
Primary DI / UDI-DI
10801902128536 FDA UDI
510(k) Number
K810675 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Peripheral artery cannula FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 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

Yes

FDA UDI

Category: Peripheral artery cannula

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

Similar devices

Also classified as Peripheral artery cannula.

Cleared under the same submission

K810675 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI b4b582ca-6a2b-4ac9-add2-5fa7c2b3e4c9 37 fields · synced May 30, 2026