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Marksman

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Marksman FDA UDI
Generic Name
Vascular microcatheter FDA UDI
Device Name
FA-55135-1030 MARKSMAN CATHETER 135CM FDA UDI
Model / Reference
FA-55135-1030 FDA UDI
Description
FA-55135-1030 MARKSMAN CATHETER 135CM FDA UDI

Identifiers

Primary DI / UDI-DI
00836462014060 FDA UDI
510(k) Number
K091559 FDA UDI
FDA Product Code
KRA FDA UDI
GMDN Term
Vascular microcatheter 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 135 Centimeter FDA UDI

Category: Vascular microcatheter

Marksman by Micro Therapeutics, 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

Sources (1)

  • FDA UDI d944574b-3bf5-4fa2-be08-dc2e7aa6338b 37 fields · synced May 30, 2026