FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479265121 · Model: 16-PAHL2.5G1.0X · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
McKesson
Primary DI
20612479265121
Version / Model
16-PAHL2.5G1.0X
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-03-30
Public Version
1
Public Version Date
2023-04-07
Public Version Status
New
Public Device Record Key
3b723b30-9333-4de0-9976-e0382bac7c5c

Device Description

LANCET, HEEL 2.5GX1.0MM

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
No
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 40612479265132
Primary 20612479265121
Unit of Use 10612479265117