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V-Guide

FDA UDI

Class I (US FDA UDI)

by RF Medical Co., Ltd.

Identity

Trade Name
V-Guide FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Model / Reference
VG1606 FDA UDI

Identifiers

Primary DI / UDI-DI
08800142923869 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Needle guide, single-use 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Needle guide, single-use

V-Guide by RF Medical Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2dfd5b1d-4644-42f8-a408-59294a96c773 32 fields · synced Jun 1, 2026