LiteTouch

FDA UDI

Class II (US FDA UDI)

by Amity Holdings, Llc

Identity

Trade Name: LiteTouch FDA UDI
Generic Name: Hypodermic needle, single-use FDA UDI
Device Name: MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/Needle FDA UDI
Model / Reference: 724LW FDA UDI
Description: MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/Needle FDA UDI

Identifiers

Primary DI / UDI-DI: 00732671072429 FDA UDI
FDA Product Code: FMI FDA UDI
FMF FDA UDI
GMDN Term: Hypodermic needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5570 FDA UDI
880.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 1.0 Inch FDA UDI
Needle Gauge — 21 Gauge FDA UDI
Total Volume — 10 Milliliter FDA UDI

Category: Hypodermic needle, single-use General-purpose syringe, single-use

LiteTouch by Amity Holdings, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Merit Medical® — Merit Medical Systems, Inc. · Class II
SOFT-JECT® — Henke-Sass, Wolf GmbH · Class II
CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
SURGYCO — Surgyco LLC · Class I
NAMIC — MEDLINE INDUSTRIES, INC. · Class II
HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
SURGYCO — Surgyco LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Amity Holdings, Llc

Sources (1)

FDA UDI 4db79130-53db-4e59-82ee-8c86384b42db 34 fields · synced Jun 1, 2026