← Back to catalogue

Arterial Catheter Mini-Kit

FDA UDI

Class I (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Arterial Catheter Mini-Kit FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
Arterial Catheter Mini-Kit 20ga x 3" FDA UDI
Model / Reference
498107 FDA UDI
Description
Arterial Catheter Mini-Kit 20ga x 3" FDA UDI

Identifiers

Catalog Number
498107 FDA UDI
Primary DI / UDI-DI
00886333215584 FDA UDI
510(k) Number
K780871 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
Peripheral vascular catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 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: Peripheral vascular catheter

Arterial Catheter Mini-Kit by Argon Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b8e91941-8925-4990-81dd-af10c8adf37f 37 fields · synced Jun 9, 2026