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TRI-JECT 3-Way IV Administration Organizer without Stopcock

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
TRI-JECT 3-Way IV Administration Organizer without Stopcock FDA UDI
Generic Name
General-purpose catheter connector, sterile FDA UDI
Device Name
TRI-JECT 3-Way IV Administration Organizer without Stopcock FDA UDI
Model / Reference
041230001A FDA UDI
Description
TRI-JECT 3-Way IV Administration Organizer without Stopcock FDA UDI

Identifiers

Catalog Number
041230001A FDA UDI
Primary DI / UDI-DI
00886333201457 FDA UDI
FDA Product Code
DRS FDA UDI
GMDN Term
General-purpose catheter connector, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2850 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

Yes

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

Yes

FDA UDI

Category: General-purpose catheter connector, sterile

TRI-JECT 3-Way IV Administration Organizer without Stopcock by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as General-purpose catheter connector, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argon Medical Devices, Inc.

Sources (1)

  • FDA UDI bb412a56-49fc-4d32-bed8-2b15a8c3a0ac 35 fields · synced Jun 9, 2026