FDA UDI In Commercial Distribution 🇺🇸 United States

LiteTouch

DI: 00732671022172 · Model: 2217 · AMITY HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
LiteTouch
Primary DI
00732671022172
Version / Model
2217
Catalog Number
2217
Company Name
AMITY HOLDINGS, LLC
Labeler DUNS
016069284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-21
Public Version
1
Public Version Date
2021-06-29
Public Version Status
New
Public Device Record Key
8185dc53-4395-4bae-af69-dd817c98eea3
Distribution End Date
2026-05-12

Device Description

Luer Lock Syringe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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 10732671122176
Primary 00732671022172
Package 20732671222170
Package 30732671322174

Customer Contacts

Phone
800 327 8894

Premarket Submissions

Submission Number Supplement Number
K132553 000

Device Sizes

Type Value Unit Text
Total Volume 50.0 Milliliter