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Mini Stick MAX

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
Mini Stick MAX FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Mini Stick MAX Coaxial Microintroducer Kit FDA UDI
Model / Reference
H965457510 FDA UDI
Description
Mini Stick MAX Coaxial Microintroducer Kit FDA UDI

Identifiers

Catalog Number
45-751 FDA UDI
Primary DI / UDI-DI
15051684022941 FDA UDI
510(k) Number
K132713 FDA UDI
FDA Product Code
DRE FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1310 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
Length — 10 Centimeter FDA UDI
Outer Diameter — 1.42 Millimeter FDA UDI
Lumen/Inner Diameter — 0.5 Millimeter FDA UDI
Catheter Gauge — 4 French FDA UDI

Category: Vascular catheter introduction set, nonimplantable

Mini Stick MAX 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.

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 f71a8d5f-bcf2-4067-9a1a-b3e71515bd90 37 fields · synced Jun 20, 2026