FDA UDI In Commercial Distribution 🇺🇸 United States

Medtlet

DI: M9923013010 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Medtlet
Primary DI
M9923013010
Version / Model
1
Catalog Number
30-13-01
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-31
Public Version
1
Public Version Date
2023-11-08
Public Version Status
New
Public Device Record Key
ab16c95f-8b84-4b19-b4b5-973842b0cd8b

Device Description

Medt Let I lancing device

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Primary M9923013010
Package M9923013013
Package M9923013015

Customer Contacts

Phone
7709356499