FDA UDI In Commercial Distribution 🇺🇸 United States

Vyaire

DI: 08809083941604 · Model: 2009111-150 · BIOPROTECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vyaire
Primary DI
08809083941604
Version / Model
2009111-150
Company Name
BIOPROTECH INC.
Labeler DUNS
688460539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-15
Public Version
1
Public Version Date
2018-12-17
Public Version Status
New
Public Device Record Key
9be2f733-2757-48b9-8685-e05bd29e78f0

Device Description

ELECTRODE, PEDIATRIC, CLOTH, ROUND, SOLID GEL, 50/POUCH

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 18809083941601
Primary 08809083941604

Premarket Submissions

Submission Number Supplement Number
K020003 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius