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Benchmark MAX System

FDA UDI

Class II (US FDA UDI)

by Penumbra, Inc.

Identity

Trade Name
Benchmark MAX System FDA UDI
Generic Name
Vascular microcatheter FDA UDI
Device Name
BMX81 105cm, 5F SIM 130cm Select FDA UDI
Model / Reference
BMX7F105SIM130-A FDA UDI
Description
BMX81 105cm, 5F SIM 130cm Select FDA UDI

Identifiers

Primary DI / UDI-DI
00815948024564 FDA UDI
510(k) Number
K221822 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular microcatheter 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

Yes

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

Category: Vascular guide-catheter, single-useVascular microcatheter

Benchmark MAX System by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular microcatheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Penumbra, Inc.

Sources (1)

  • FDA UDI f73b9bd4-8757-4566-a351-8dc7f7204310 34 fields · synced May 30, 2026