FDA UDI In Commercial Distribution 🇺🇸 United States

Fisher & Paykel Healthcare

DI: 09420012467560 · Model: MYAIRVOCHAMBER1 · FISHER & PAYKEL HEALTHCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fisher & Paykel Healthcare
Primary DI
09420012467560
Version / Model
MYAIRVOCHAMBER1
Catalog Number
MYAIRVOCHAMBER1
Company Name
FISHER & PAYKEL HEALTHCARE LIMITED
Labeler DUNS
590153276
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-23
Public Version
1
Public Version Date
2022-05-31
Public Version Status
New
Public Device Record Key
fdb4cc75-0a73-499f-9261-462622e59fc4

Device Description

myAirvo Reusable Chamber

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZD Ventilator, Non-Continuous (Respirator)

GMDN Terms

Code Name
60662 Inspiratory line humidification chamber, reusable

Identifiers

Type ID
Package 09420012467577
Primary 09420012467560

Premarket Submissions

Submission Number Supplement Number
K131895 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius