FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 20885380102803 · Model: SLPBHN200 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
20885380102803
Version / Model
SLPBHN200
Catalog Number
SLPBHN200
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2019-05-03
Public Version
2
Public Version Date
2023-05-24
Public Version Status
Update
Public Device Record Key
bf548c22-3a14-4b1f-9e1c-1e70ae497342

Device Description

PUSH BUTTOM ACTIVATED FINGER LANCET

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
FMK Lancet, blood

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 50885380102804
Primary 20885380102803
Unit of Use 10885380102806