FDA UDI In Commercial Distribution 🇺🇸 United States

HEART™

DI: 10889483223734 · Model: 100619 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
HEART™
Primary DI
10889483223734
Version / Model
100619
Catalog Number
100619
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-15
Public Version
2
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
78173870-be25-4167-84af-664253f6e783

Device Description

HEART™ Direct Connect Continuous Nebulizer, Adult Aerosol Mask, 8' Corrugated Tubing

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
31309 Nebulizing system delivery set, single-use

Identifiers

Type ID
Primary 10889483223734
Previous 00709078000119
Package 20889483223731

Customer Contacts