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FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Epidural anaesthesia set, medicated FDA UDI
Device Name
FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit FDA UDI
Model / Reference
IPN925044 FDA UDI
Description
FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit FDA UDI

Identifiers

Catalog Number
NYU-05500-1 FDA UDI
Primary DI / UDI-DI
10801902210279 FDA UDI
510(k) Number
K140110 FDA UDI
FDA Product Code
BSO FDA UDI
GMDN Term
Epidural anaesthesia set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 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
MRI Safety
MR Unsafe FDA UDI

Category: Epidural anaesthesia set, medicated

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

Similar devices

Also classified as Epidural anaesthesia set, medicated.

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 c9a965d5-d919-4f24-81b1-281cb34c8951 37 fields · synced May 30, 2026