← Back to catalogue

Kmedic

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
KMEDIC FDA UDI
Generic Name
Endometrial biopsy curette FDA UDI
Device Name
KEVORKIEN YOUNGE CURETTE. 12" WITHOUT BASKET FDA UDI
Model / Reference
IPN015572 FDA UDI
Description
KEVORKIEN YOUNGE CURETTE. 12" WITHOUT BASKET FDA UDI

Identifiers

Catalog Number
KM64796 FDA UDI
Primary DI / UDI-DI
24026704290257 FDA UDI
FDA Product Code
HCY FDA UDI
GMDN Term
Endometrial biopsy curette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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 — 305 Millimeter FDA UDI

Category: Endometrial biopsy curette

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

Similar devices

Also classified as Endometrial biopsy curette.

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 f7dea735-9dd3-425c-854b-f7d2ebd037f2 36 fields · synced May 30, 2026