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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 System FDA UDI
Model / Reference
MC*PB2413ZRC FDA UDI
Description
PROGREAT Microcatheter System FDA UDI

Identifiers

Catalog Number
MC*PB2413ZRC FDA UDI
Primary DI / UDI-DI
04987350738264 FDA UDI
FDA Product Code
DQO FDA UDI
KRA FDA UDI
GMDN Term
Vascular microcatheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
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
Length — 130 Centimeter FDA UDI
Outer Diameter — 0.8 Millimeter FDA UDI
Lumen/Inner Diameter — 0.57 Millimeter 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI 51aec4f5-2d84-4248-81b8-bdb67a2ab186 37 fields · synced Jun 7, 2026