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StarBurst

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
StarBurst FDA UDI
Generic Name
Non-vascular catheter introduction set FDA UDI
Device Name
Starburst Access System FDA UDI
Model / Reference
700102331 FDA UDI
Description
Starburst Access System FDA UDI

Identifiers

Primary DI / UDI-DI
H7877001023310 FDA UDI
FDA Product Code
GEI FDA UDI
KGZ FDA UDI
GMDN Term
Non-vascular catheter introduction set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
878.4200 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 — 11 Centimeter FDA UDI

Category: Non-vascular catheter introduction set

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

Similar devices

Also classified as Non-vascular catheter introduction set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiodynamics, Inc

Sources (1)

  • FDA UDI 812ee8be-9f7c-47f9-b5ce-e21a10918a17 35 fields · synced Jun 20, 2026