FDA UDI In Commercial Distribution 🇺🇸 United States

Vibralung Patient Kit

DI: 00709078001369 · Model: 9600 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vibralung Patient Kit
Primary DI
00709078001369
Version / Model
9600
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
61c20187-a756-4992-8b4c-e23414e4efce

Device Description

1 each: Standard Y Adapter, Aerosol Y-Adapter, Hand-held Transducer (HHT) assembly with screw-on Cone pre-attached, and disposable ear plugs.

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
Yes
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
No
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
45335 Electroacoustical airway secretion-clearing system

Identifiers

Type ID
Primary 00709078001369
Package 10709078001366

Premarket Submissions

Submission Number Supplement Number
K133057 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 93 Percent (%) Relative Humidity