FDA UDI In Commercial Distribution 🇺🇸 United States

Bellavista

DI: 10190752188853 · Model: 301.114.000 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bellavista
Primary DI
10190752188853
Version / Model
301.114.000
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-02
Public Version
1
Public Version Date
2024-01-10
Public Version Status
New
Public Device Record Key
aeaccea9-530a-4280-91d0-c55bc461fad8

Device Description

Diagnostic Package Capnography Mainstream

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
MR Unsafe
Direct Marking Exempt
No
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
CBK Ventilator, Continuous, Facility Use

GMDN Terms

Code Name
36552 Patient monitoring system module, carbon dioxide
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 10190752188853

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183364 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
40 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 120 KiloPascal