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Needle Guide

FDA UDIEUDAMED

Class I (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Needle Guide FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
Needle Guide for Lorad Stereo Loc for 16ga - 19ga FDA UDI
Model / Reference
LNGO1619PX FDA UDI
Description
Needle Guide for Lorad Stereo Loc for 16ga - 19ga FDA UDI

Identifiers

Catalog Number
LNGO1619PX FDA UDI
Primary DI / UDI-DI
00886333001682 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Needle guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Needle guide, single-use

Needle Guide by Argon Medical Devices, Inc. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 31ed8d67-44b6-49b9-a4c3-4584bba526ef 37 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026