FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479185019 · Model: 16-89144 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479185019
Version / Model
16-89144
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-15
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
432384be-f586-419b-b3a0-9e508925e509

Device Description

DRESSING, ISLAND BARRIER STR WTRPRF 4X4 ST

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Package 20612479185023
Primary 10612479185019
Package 40612479185034