FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 30884389103085 · Model: MPHSAFETY23 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
Medline
Primary DI
30884389103085
Version / Model
MPHSAFETY23
Catalog Number
MPHSAFETY23
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2023-01-21
Public Version
1
Public Version Date
2023-01-30
Public Version Status
New
Public Device Record Key
0aeda56f-66a4-4d5b-a073-02236b6f723c

Device Description

LANCET,SAFETY,23G,1.8MM,PUSH BUTTON

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
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
61579 Blood lancet, single-use

Identifiers

Type ID
Package 40884389103082
Primary 30884389103085
Unit of Use 10884389103081

Customer Contacts