FDA UDI In Commercial Distribution 🇺🇸 United States

LCH

DI: M99208013103P120LCH3 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
120

Basic Information

Brand Name
LCH
Primary DI
M99208013103P120LCH3
Version / Model
1
Catalog Number
08-01-3103P-120LCH
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2025-06-23
Public Version
1
Public Version Date
2025-07-01
Public Version Status
New
Public Device Record Key
5ba942fa-45e3-49bf-911d-b2fe0b8c936b

Device Description

Insulin syringe 1ml 31G x 5/16" 8mm

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
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
FMF Syringe, Piston

GMDN Terms

Code Name
38501 Insulin syringe/needle, basic

Identifiers

Type ID
Unit of Use M99208013103P120LCH0
Primary M99208013103P120LCH3
Package M99208013103P120LCH5

Customer Contacts

Phone
7709356499