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PulseSpray

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
PulseSpray FDA UDI
Generic Name
Peripheral vascular intervention infusion catheter FDA UDI
Device Name
PulseSpray Infusion System FDA UDI
Model / Reference
H787125004190 FDA UDI
Description
PulseSpray Infusion System FDA UDI

Identifiers

Catalog Number
12500419 FDA UDI
Primary DI / UDI-DI
15051684013253 FDA UDI
510(k) Number
K163356 FDA UDI
FDA Product Code
KRA FDA UDI
GMDN Term
Peripheral vascular intervention infusion catheter 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 90 Centimeter FDA UDI
Catheter Gauge — 3 French FDA UDI

Category: Peripheral vascular intervention infusion catheter

PulseSpray by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular intervention infusion catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiodynamics, Inc

Sources (1)

  • FDA UDI 070c3cdf-8ffe-4574-a2fe-35fba2fe9c5d 38 fields · synced Jun 20, 2026