FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479281704 · Model: 199-138 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
McKesson
Primary DI
10612479281704
Version / Model
199-138
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-20
Public Version
1
Public Version Date
2026-01-28
Public Version Status
New
Public Device Record Key
067963bb-89d6-49b9-994d-0f2d96000b2c

Device Description

Manuka Honey 4 in x 5 in gauze sheet, non adherant

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
FRO Dressing, Wound, Drug

GMDN Terms

Code Name
47203 Wound-nonadherent dressing, permeable, antimicrobial

Identifiers

Type ID
Package 20612479281718
Primary 10612479281704
Package 40612479281729

Premarket Submissions

Submission Number Supplement Number
K110042 000