FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479204383 · Model: 339 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479204383
Version / Model
339
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-09
Public Version
4
Public Version Date
2023-10-16
Public Version Status
Update
Public Device Record Key
44a0e8c0-ca90-4e4e-b983-0194f299b9b0

Device Description

SOLUTION, GLUT 2.6% 14DAY QT

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
MED Sterilant, Medical Devices

GMDN Terms

Code Name
40579 Glutaraldehyde device sterilant

Identifiers

Type ID
Primary 10612479204383
Package 40612479204391