FDA UDI In Commercial Distribution 🇺🇸 United States

LiteTouch

DI: 00732671021137 · Model: 2113 · AMITY HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
LiteTouch
Primary DI
00732671021137
Version / Model
2113
Catalog Number
2113
Company Name
AMITY HOLDINGS, LLC
Labeler DUNS
016069284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-18
Public Version
2
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
39a2ee1e-5f99-4359-a808-326195b62033
Distribution End Date
2026-02-18

Device Description

MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/o Needle

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMF Syringe, Piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 10732671121131
Primary 00732671021137
Package 20732671221135
Package 30732671321139

Customer Contacts

Phone
8003278894

Device Sizes

Type Value Unit Text
Total Volume 1 Milliliter