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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Endometrial biopsy curette FDA UDI
Device Name
Affinity KEVORKIAN-YOUNGE ENDOCERVICAL BIOPSY CURETTE, SLIGHTLY CVD OVERALL LENGTH 12 inches 30.5CM FDA UDI
Model / Reference
GA1775 FDA UDI
Description
Affinity KEVORKIAN-YOUNGE ENDOCERVICAL BIOPSY CURETTE, SLIGHTLY CVD OVERALL LENGTH 12 inches 30.5CM FDA UDI

Identifiers

Catalog Number
GA1775 FDA UDI
Primary DI / UDI-DI
10885403042485 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endometrial biopsy curette

V. Mueller by Steris Corporation — 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

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 083c5669-f81a-496f-b239-2fe5a945f8cb 35 fields · synced Jun 8, 2026