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R2P Destination Slender

FDA UDI

Class II (US FDA UDI)

by Terumo Medical Corporation

Identity

Trade Name
R2P Destination Slender FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
R2P Destination Slender Guiding Sheath FDA UDI
Model / Reference
GS-R6ST1C75W FDA UDI
Description
R2P Destination Slender Guiding Sheath FDA UDI

Identifiers

Catalog Number
GS-R6ST1C75W FDA UDI
Primary DI / UDI-DI
00389701012360 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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
Length — 75 Centimeter FDA UDI
Catheter Gauge — 6 French FDA UDI

Category: Vascular guide-catheter, single-use

R2P Destination Slender by Terumo Medical Corporation — 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 Medical Corporation

Sources (1)

  • FDA UDI 504fb912-3efe-4418-b7af-78febdd2863d 37 fields · synced May 30, 2026