FDA UDI In Commercial Distribution 🇺🇸 United States

AirFlow™

DI: 10889483631539 · Model: AF5102MC-P · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirFlow™
Primary DI
10889483631539
Version / Model
AF5102MC-P
Catalog Number
AF5102MC-P
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-31
Public Version
1
Public Version Date
2025-02-10
Public Version Status
New
Public Device Record Key
fad3f562-bd17-4da5-81c8-e21f947a4523

Device Description

AirFlow™ Adult Resuscitator with Integrated Manometer, 40cm Pop-Off, Corrugated Tubing and PEEP Valve

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BTM Ventilator, Emergency, Manual (Resuscitator)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 30889483631533
Primary 10889483631539

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-18 – 51 Degrees Celsius