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PASV MS Kit

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc.

Identity

Trade Name
PASV MS Kit FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
PASV MS Kit with Pressure Activated Safety Valve with 3.5F x 5cm Dilator FDA UDI
Model / Reference
M001MS3K0 FDA UDI
Description
PASV MS Kit with Pressure Activated Safety Valve with 3.5F x 5cm Dilator FDA UDI

Identifiers

Catalog Number
MS3K FDA UDI
Primary DI / UDI-DI
15051684019880 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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
Catheter Gauge — 3.5 French FDA UDI
Length — 5 Centimeter FDA UDI

Category: Vascular catheter introduction set, nonimplantable

PASV MS Kit by Angiodynamics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiodynamics, Inc.

Sources (1)

  • FDA UDI 1b51eaa6-ea3d-4fe9-9605-ae36a2cabc20 36 fields · synced Jun 8, 2026