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Guide Wire M

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
GUIDE WIRE M FDA UDI
Generic Name
General-purpose non-vascular guidewire FDA UDI
Device Name
RADIFOCUS GUIDE WIRE M Tapered Gold FDA UDI
Model / Reference
GM1602 FDA UDI
Description
RADIFOCUS GUIDE WIRE M Tapered Gold FDA UDI

Identifiers

Catalog Number
RF*RB16188TA FDA UDI
Primary DI / UDI-DI
04987350774132 FDA UDI
FDA Product Code
DQX FDA UDI
GCJ FDA UDI
GMDN Term
General-purpose non-vascular guidewire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 FDA UDI
876.1500 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
Outer Diameter — 0.41 Millimeter FDA UDI
Length — 180 Centimeter FDA UDI

Category: Cardiac/peripheral vascular guidewire, single-useGeneral-purpose non-vascular guidewire

Guide Wire M by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose non-vascular guidewire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI 125f8045-cb4a-46ea-a31e-404405b96130 37 fields · synced May 30, 2026