FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479135564 · Model: 16-602318 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479135564
Version / Model
16-602318
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-09
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
37c763c3-3b3b-453f-9004-d0195b11f393

Device Description

All-Purpose Sponge, Sterile, 2” x 2", 4-Ply

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
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 20612479135578
Primary 10612479135564
Package 40612479135589