FDA UDI In Commercial Distribution 🇺🇸 United States

Bellavista

DI: 10190752148888 · Model: 302.231.001 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bellavista
Primary DI
10190752148888
Version / Model
302.231.001
Catalog Number
302.231.001
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-04
Public Version
1
Public Version Date
2022-04-12
Public Version Status
New
Public Device Record Key
4749c156-6a13-405d-8d9c-4f18cfded228

Device Description

Exhalation Valve

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
42411 Neonatal/adult intensive-care ventilator

Identifiers

Type ID
Package 70190752148880
Primary 10190752148888

Customer Contacts