FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479262106 · Model: 16-4960 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
48

Basic Information

Brand Name
McKesson
Primary DI
20612479262106
Version / Model
16-4960
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
48
Record Status
Published
Publish Date
2022-09-28
Public Version
1
Public Version Date
2022-10-06
Public Version Status
New
Public Device Record Key
baf60e71-3857-41ca-814a-49790ebd2387

Device Description

UltraSound Gel Clear 20g pouch

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
MUI Media, Coupling, Ultrasound

GMDN Terms

Code Name
58735 Topical coupling gel, sterile

Identifiers

Type ID
Package 40612479262117
Primary 20612479262106
Unit of Use 10612479262147

Premarket Submissions

Submission Number Supplement Number
K130581 000