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FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Peripheral anaesthesia single-administration set, non-medicated FDA UDI
Device Name
19 Ga. x 60 cm StimuCath(R) Continuous Nerve Block Set FDA UDI
Model / Reference
IPN040008 FDA UDI
Description
19 Ga. x 60 cm StimuCath(R) Continuous Nerve Block Set FDA UDI

Identifiers

Catalog Number
AB-05060 FDA UDI
Primary DI / UDI-DI
00801902028341 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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

No

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
Length — 60 Centimeter FDA UDI

Category: Peripheral anaesthesia single-administration set, non-medicated

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

Similar devices

Also classified as Peripheral anaesthesia single-administration set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI fbaa9099-9d58-4a3d-97ec-d9a0f48f5e9e 36 fields · synced May 31, 2026