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Finecross

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
FINECROSS FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
FINECROSS MG Coronary Micro-Guide Catheter FDA UDI
Model / Reference
35-1450 FDA UDI
Description
FINECROSS MG Coronary Micro-Guide Catheter FDA UDI

Identifiers

Catalog Number
NC*F865A FDA UDI
Primary DI / UDI-DI
04987350703187 FDA UDI
FDA Product Code
KRA FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1210 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 — 0.60 Millimeter FDA UDI
Length — 150 Centimeter FDA UDI

Category: Vascular guide-catheter, single-use

Finecross 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 40b2baba-6d79-472d-92f7-831109166f2b 37 fields · synced Jun 8, 2026