FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 00612479261440 · Model: 18-3300M · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
00612479261440
Version / Model
18-3300M
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-28
Public Version
2
Public Version Date
2022-02-09
Public Version Status
Update
Public Device Record Key
04a2f8a0-5785-4a06-b1ed-608bf30fd798

Device Description

Universal Securement Device MEDIUM | 3.5 in (100/bx, 10/ mstcs)

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder

Identifiers

Type ID
Package 00612479261457
Primary 00612479261440
Package 00612479262164