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Kmedic

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
KMEDIC FDA UDI
Generic Name
Wire holding/twisting pliers FDA UDI
Device Name
PLIERS, NEEDLE NOSE 7" LONG JAW FDA UDI
Model / Reference
IPN014520 FDA UDI
Description
PLIERS, NEEDLE NOSE 7" LONG JAW FDA UDI

Identifiers

Catalog Number
KM48250 FDA UDI
Primary DI / UDI-DI
24026704278460 FDA UDI
FDA Product Code
HTC FDA UDI
GMDN Term
Wire holding/twisting pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 17.8 Centimeter FDA UDI

Category: Wire holding/twisting pliers

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

Similar devices

Also classified as Wire holding/twisting pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 7a1d9f87-f28e-4b6d-afb5-d63a0bb844d0 36 fields · synced Jun 8, 2026