FDA UDI In Commercial Distribution 🇺🇸 United States

Medtfine

DI: M9923012303 · 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
Medtfine
Primary DI
M9923012303
Version / Model
1
Catalog Number
30-12-30
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
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
6baaa7bb-cdfb-4c14-bbc1-e5a73ae45ac6

Device Description

Pull Top lancet 30G

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
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Package M9923012305
Primary M9923012303
Unit of Use M9923012300

Customer Contacts

Phone
7709356499

Device Sizes

Type Value Unit Text
Needle Gauge 30 Gauge