← Back to catalogue

Kmedic

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
KMEDIC FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
KERRISON PUNCH THIN FOOT PLATE 7" FORWARD 5MM FDA UDI
Model / Reference
IPN015322 FDA UDI
Description
KERRISON PUNCH THIN FOOT PLATE 7" FORWARD 5MM FDA UDI

Identifiers

Catalog Number
KM55917 FDA UDI
Primary DI / UDI-DI
24026704287660 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 18 Centimeter FDA UDI

Category: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI d664c9c7-aaa7-476a-8758-250f7c6db87c 36 fields · synced Jun 6, 2026