FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479203710 · Model: 32630 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
20612479203710
Version / Model
32630
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-21
Public Version
1
Public Version Date
2020-07-29
Public Version Status
New
Public Device Record Key
a6f4b170-c7f7-4f3e-86d5-7af3e40d4fbd

Device Description

Bubble Humidifier PRESSURE RELIEF VALVE | SINGLE PATIENT USE

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

GMDN Terms

Code Name
35113 Non-heated respiratory humidifier

Identifiers

Type ID
Package 40612479203721
Primary 20612479203710