FDA UDI In Commercial Distribution 🇺🇸 United States

MedtLancet

DI: M992302228183 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
MedtLancet
Primary DI
M992302228183
Version / Model
1
Catalog Number
30-22-2818
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-11-01
Public Version
1
Public Version Date
2023-11-09
Public Version Status
New
Public Device Record Key
4bc1e618-ebbd-4aa7-bafc-49c34979b7ff

Device Description

Safety lancet 28G*1.8mm

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
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package M992302228185
Primary M992302228183
Unit of Use M992302228180

Customer Contacts

Phone
7709356499

Device Sizes

Type Value Unit Text
Needle Gauge 28 Gauge