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Double Male LL Adapter

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Double Male LL Adapter FDA UDI
Generic Name
General-purpose catheter connector, sterile FDA UDI
Device Name
Double Male LL Adapter Special Adapter to Convert a Female Fitting to Male LL FDA UDI
Model / Reference
040184000A FDA UDI
Description
Double Male LL Adapter Special Adapter to Convert a Female Fitting to Male LL FDA UDI

Identifiers

Catalog Number
040184000A FDA UDI
Primary DI / UDI-DI
00886333201044 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

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

Yes

FDA UDI

Category: General-purpose catheter connector, sterile

Double Male LL Adapter by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 eca3d3ec-0ca6-4958-bcb0-c0f2cf7dfb54 35 fields · synced Jun 9, 2026