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Kmedic

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
KMEDIC FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
RONGEURS CASPAR INTRAVERTEBRAL DISK 4 X 14 MILLIMETER STRAIGHT 7.25" FDA UDI
Model / Reference
IPN015346 FDA UDI
Description
RONGEURS CASPAR INTRAVERTEBRAL DISK 4 X 14 MILLIMETER STRAIGHT 7.25" FDA UDI

Identifiers

Catalog Number
KM55962 FDA UDI
Primary DI / UDI-DI
24026704287905 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 18.4 Centimeter FDA UDI

Category: Spinal rongeur

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

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 11040037-1708-481b-8c27-1dbb48879ac3 36 fields · synced May 31, 2026