← Back to catalogue

LiteTouch

FDA UDI

Class II (US FDA UDI)

by Amity Holdings, Llc

Identity

Trade Name
LiteTouch FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/o Needle - Bulk Pack -Trays FDA UDI
Model / Reference
2111 FDA UDI
Description
MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/o Needle - Bulk Pack -Trays FDA UDI

Identifiers

Catalog Number
2111 FDA UDI
Primary DI / UDI-DI
00732671021113 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Category: 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.

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

Manufacturer
Amity Holdings, Llc

Sources (1)

  • FDA UDI a3ef6f30-6a0a-4fdc-be7c-914bc6de7f19 37 fields · synced May 30, 2026