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Navicross

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
NAVICROSS FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
NAVICROSS Support Catheter FDA UDI
Model / Reference
NC18651 FDA UDI
Description
NAVICROSS Support Catheter FDA UDI

Identifiers

Catalog Number
PN*NA180G3H FDA UDI
Primary DI / UDI-DI
04987892077197 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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 — 0.85 Millimeter FDA UDI
Length — 65 Centimeter FDA UDI

Category: Vascular guide-catheter, single-use

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

Similar devices

Also classified as Vascular guide-catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI b0d3519d-3c87-4fce-805b-bf86388d4ea1 37 fields · synced May 30, 2026