FDA UDI In Commercial Distribution 🇺🇸 United States

Meijer

DI: 00713733905015 · Model: AT 0435ME · MEIJER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Meijer
Primary DI
00713733905015
Version / Model
AT 0435ME
Company Name
MEIJER, INC.
Labeler DUNS
006959555
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-07-31
Public Version
1
Public Version Date
2023-08-08
Public Version Status
New
Public Device Record Key
9798cd8f-6097-42ec-a40e-bc58f458c42b

Device Description

Meijer Lancets - Thin, 26G

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
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
No
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
45142 Blood lancing device tip

Identifiers

Type ID
Package 30713733905016
Primary 00713733905015
Unit of Use 00384700435011

Device Sizes

Type Value Unit Text
Needle Gauge 26 Gauge