FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479135219 · Model: 16-40334 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
McKesson
Primary DI
20612479135219
Version / Model
16-40334
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2020-06-10
Public Version
2
Public Version Date
2022-10-25
Public Version Status
Update
Public Device Record Key
e0e38ed5-18da-4b5b-a3fa-9a9c8b55ac47

Device Description

Non-Woven Sponge, Non-Sterile, 3" x 3", High Absorbency, 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
No
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 40612479135220
Primary 20612479135219
Unit of Use 10612479234793