FDA UDI In Commercial Distribution 🇺🇸 United States

Ventlab, LLC

DI: 10889483104200 · Model: AF5140MC-P · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ventlab, LLC
Primary DI
10889483104200
Version / Model
AF5140MC-P
Catalog Number
AF5140MC-P
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-20
Public Version
1
Public Version Date
2023-06-28
Public Version Status
New
Public Device Record Key
46fb57d4-bd59-4573-9314-2b0503f5e8fe

Device Description

AirFlow Adult Resuscitator with Integrated Manometer, B/V Filter, Corrugated Tubing, Mask, 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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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 30889483104204
Primary 10889483104200

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 1500 Milliliter