FDA UDI In Commercial Distribution 🇺🇸 United States

LCH

DI: M99230403160120LCH3 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
120

Basic Information

Brand Name
LCH
Primary DI
M99230403160120LCH3
Version / Model
1
Catalog Number
30-40-3160-120LCH
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2026-03-04
Public Version
1
Public Version Date
2026-03-12
Public Version Status
New
Public Device Record Key
e46ee646-1ee5-4178-8737-392cc5ced40f

Device Description

Pen needle 31G*6mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
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
44127 Autoinjector needle

Identifiers

Type ID
Package M99230403160120LCH5
Primary M99230403160120LCH3
Unit of Use M99230403160120LCH0

Customer Contacts

Phone
7709356499

Device Sizes

Type Value Unit Text
Needle Gauge 31 Gauge