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FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, non-silicone FDA UDI
Device Name
EZ-Stabilizer FDA UDI
Model / Reference
IPN033748 FDA UDI
Description
EZ-Stabilizer FDA UDI

Identifiers

Catalog Number
9066-VC-005 FDA UDI
Primary DI / UDI-DI
10816000012557 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, non-silicone FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Dressing-fixation skin adhesive tape, non-silicone

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

Similar devices

Also classified as Dressing-fixation skin adhesive tape, non-silicone.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d0274bc-be06-42d5-ab38-2e2b670dff4d 36 fields · synced Jun 8, 2026