Kmedic

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: KMEDIC FDA UDI
Generic Name: Nerve/vessel retractor FDA UDI
Device Name: SCOVILLE NERVE ROOT RETRACTOR 9 1/4" ANGLED FDA UDI
Model / Reference: IPN015197 FDA UDI
Description: SCOVILLE NERVE ROOT RETRACTOR 9 1/4" ANGLED FDA UDI

Identifiers

Catalog Number: KM55426 FDA UDI
Primary DI / UDI-DI: 24026704286397 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Nerve/vessel retractor 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Width — 8 Millimeter FDA UDI
Length — 20.3 Centimeter FDA UDI

Category: Nerve/vessel retractor

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 164748e2-81a4-4bf2-b2fd-fb70c93fd982 36 fields · synced Jun 6, 2026