FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20197344112705 · Model: MPHSTSIDE23 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
MEDLINE
Primary DI
20197344112705
Version / Model
MPHSTSIDE23
Catalog Number
MPHSTSIDE23
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2024-10-25
Public Version
1
Public Version Date
2024-11-04
Public Version Status
New
Public Device Record Key
203714dc-d816-43d2-b461-990eb5d08dae

Device Description

LANCET,SAFETY,23G,1.8MM,SIDE 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
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
FMK Single use only blood lancet with an integral sharps injury prevention feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 30197344112702
Primary 20197344112705
Unit of Use 10197344112708

Customer Contacts