FDA UDI In Commercial Distribution 🇺🇸 United States

Meijer

DI: 50760236326705 · Model: MJ38220 · MEIJER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Meijer
Primary DI
50760236326705
Version / Model
MJ38220
Catalog Number
MJ38220
Company Name
MEIJER, INC.
Labeler DUNS
006959555
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2022-02-24
Public Version
1
Public Version Date
2022-03-04
Public Version Status
New
Public Device Record Key
2c5d20d2-fb0b-4ec2-aba2-dbc5b2478ebd

Device Description

MASK,FACE,X-SMALL,EARLOOPS,BLUE,20CT

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FXX Mask, Surgical

GMDN Terms

Code Name
35177 Surgical/medical face mask, single-use

Identifiers

Type ID
Unit of Use 00760236326700
Primary 50760236326705