Progreat

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name: PROGREAT FDA UDI
Generic Name: Vascular microcatheter FDA UDI
Device Name: PROGREAT Microcatheter Coaxial System FDA UDI
Model / Reference: MC*PP24151YW FDA UDI
Description: PROGREAT Microcatheter Coaxial System FDA UDI

Identifiers

Catalog Number: MC*PP24151YW FDA UDI
Primary DI / UDI-DI: 04987350735300 FDA UDI
FDA Product Code: DQO FDA UDI
GMDN Term: Vascular microcatheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 0.8 Millimeter FDA UDI
Lumen/Inner Diameter — 0.57 Millimeter FDA UDI
Length — 150 Centimeter FDA UDI

Category: Vascular microcatheter

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

Similar devices

Also classified as Vascular microcatheter.

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Renegade™ HI-FLO™ Kit — Boston Scientific · Class II
PROWLER — Medos International Sàrl · Class II
Merit Maestro® — Merit Medical Systems, Inc. · Class II
Lantern Delivery Catheter — PENUMBRA, INC. · Class II
Direxion™ Fathom™-16 System — Boston Scientific · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Terumo Corp.

Sources (1)

FDA UDI 18e7fe49-f3af-4e68-b30a-c02f026ced6a 37 fields · synced May 31, 2026