FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20197344111838 · Model: MPH100023 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
MEDLINE
Primary DI
20197344111838
Version / Model
MPH100023
Catalog Number
MPH100023
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-10-22
Public Version
1
Public Version Date
2025-10-30
Public Version Status
New
Public Device Record Key
38d5af73-7191-483b-8fc5-c62f37c59bbe

Device Description

LANCET, GENERAL PURPOSE, 23G

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
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
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 30197344111835
Primary 20197344111838
Unit of Use 10197344111831

Customer Contacts