FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479204048 · Model: 16-835V2 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479204048
Version / Model
16-835V2
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b010e753-edc9-4067-b328-6fcbb5e487a2

Device Description

Hand Held Pulse Oximeter - Pediatric

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
17148 Pulse oximeter, line-powered

Identifiers

Type ID
Primary 10612479204048
Package 20612479202355
Package 40612479202366