FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479137688 · Model: 19-11004 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
McKesson
Primary DI
20612479137688
Version / Model
19-11004
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-04-09
Public Version
1
Public Version Date
2020-04-17
Public Version Status
New
Public Device Record Key
734aaa9a-b448-44c5-b9dc-afb9387d52ab

Device Description

Vessel Loops MINI | WHITE

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
Yes
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
KDC Instrument, Surgical, Disposable

GMDN Terms

Code Name
36082 Medical/surgical string

Identifiers

Type ID
Package 40612479137699
Primary 20612479137688
Unit of Use 10612479137674