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EndoCurette

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
EndoCurette FDA UDI
Generic Name
Endometrial biopsy curette FDA UDI
Device Name
Endometrial Suction Curette with Syringe FDA UDI
Model / Reference
Clear FDA UDI
Description
Endometrial Suction Curette with Syringe FDA UDI

Identifiers

Catalog Number
CUR-120 FDA UDI
Primary DI / UDI-DI
H671CUR1200 FDA UDI
510(k) Number
K000974 FDA UDI
FDA Product Code
HHK FDA UDI
GMDN Term
Endometrial biopsy curette FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 27 Centimeter FDA UDI
Outer Diameter — 3.1 Millimeter FDA UDI

Category: Endometrial biopsy curette

EndoCurette by Utah Medical Products, Inc. — Class II — 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

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Manufacturer

Manufacturer
Utah Medical Products, Inc.

Sources (1)

  • FDA UDI 6d360084-eda5-4d97-a254-f1731e086503 37 fields · synced Jun 9, 2026