FDA UDI In Commercial Distribution 🇺🇸 United States

AirPhysio

DI: B99893699980215050 · Model: 1 · AIRPHYSIO PTY. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AirPhysio
Primary DI
B99893699980215050
Version / Model
1
Company Name
AIRPHYSIO PTY. LTD.
Labeler DUNS
744023767
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-22
Public Version
1
Public Version Date
2024-01-30
Public Version Status
New
Public Device Record Key
08bb5111-b497-4476-97d9-3fb1f8ee9595

Device Description

mucus clearance average lung capacity, OPEP, non invitro, no chemicals, contains one steel ball bearing TEAL coloured box

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BYI Percussor, Powered-Electric

GMDN Terms

Code Name
43947 Positive pressure airway secretion-clearing device

Identifiers

Type ID
Primary B99893699980215050

Premarket Submissions

Submission Number Supplement Number
K203209 000