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Surefire Spark Infusion System

FDA UDI

Class II (US FDA UDI)

by Surefire Medical, Inc.

Identity

Trade Name
Surefire Spark Infusion System FDA UDI
Generic Name
Peripheral vascular intervention infusion catheter FDA UDI
Device Name
150cm 0.021" Microcatheter w/ 1.5-3.5mm Expandable Tip FDA UDI
Model / Reference
SPARK-A150 FDA UDI
Description
150cm 0.021" Microcatheter w/ 1.5-3.5mm Expandable Tip FDA UDI

Identifiers

Primary DI / UDI-DI
00857136004163 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Peripheral vascular intervention infusion catheter 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 150 Centimeter FDA UDI
Lumen/Inner Diameter — 0.021 Inch FDA UDI

Category: Peripheral vascular intervention infusion catheter

Surefire Spark Infusion System by Surefire Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular intervention infusion catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surefire Medical, Inc.

Sources (1)

  • FDA UDI fd9f42ae-6e2e-4361-afad-d7507d0326f9 34 fields · synced May 30, 2026