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Needle Guide

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Needle Guide FDA UDI
Generic Name
Needle guide, reusable FDA UDI
Device Name
Reusable non-sterile endocavity needle guide with cleaning brushes (5) for use with Siemens 6.5EV13, 6.5EV13+, 6.5EV13S AND EV9-4 (on SONOLINE G20, G50, G60 S systems) transducers FDA UDI
Model / Reference
04392143 FDA UDI
Description
Reusable non-sterile endocavity needle guide with cleaning brushes (5) for use with Siemens 6.5EV13, 6.5EV13+, 6.5EV13S AND EV9-4 (on SONOLINE G20, G50, G60 S systems) transducers FDA UDI

Identifiers

Catalog Number
04392143 FDA UDI
Primary DI / UDI-DI
00841436100663 FDA UDI
510(k) Number
K875240 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Needle guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 7.4 Inch FDA UDI
Width — 1.2 Inch FDA UDI

Category: Needle guide, reusable

Needle Guide by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7fefcc32-d44a-4a41-8c55-06f4db5158a2 37 fields · synced Jun 8, 2026