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MicroStic Plus

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
MicroStic Plus FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
MicroStic Plus w/ SS Wire 4F FDA UDI
Model / Reference
497880 FDA UDI
Description
MicroStic Plus w/ SS Wire 4F FDA UDI

Identifiers

Catalog Number
497880 FDA UDI
Primary DI / UDI-DI
00886333215430 FDA UDI
510(k) Number
K780126 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

Yes

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

Yes

FDA UDI

Category: Vascular catheter introduction set, nonimplantable

MicroStic Plus by Argon Medical Devices, 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

Sources (1)

  • FDA UDI 00c5599d-598f-40d8-8f21-4b0bd817985c 37 fields · synced Jun 9, 2026