FDA UDI In Commercial Distribution 🇺🇸 United States

LiteTouch

DI: 00732671006028 · Model: 602 · AMITY HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
LiteTouch
Primary DI
00732671006028
Version / Model
602
Catalog Number
602
Company Name
AMITY HOLDINGS, LLC
Labeler DUNS
016069284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-17
Public Version
3
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
d9cda4fa-2635-4fb6-a627-2122e2307c86
Distribution End Date
2025-12-17

Device Description

Safety 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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 10732671106022
Primary 00732671006028
Package 20732671206026
Package 30732671306020

Customer Contacts

Phone
8003278894

Device Sizes

Type Value Unit Text
Needle Gauge 25 Gauge
Length 1.0 Inch