FDA UDI In Commercial Distribution 🇺🇸 United States

Ventlab

DI: 10889483074602 · Model: 301-P3052 · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ventlab
Primary DI
10889483074602
Version / Model
301-P3052
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
bb379805-4219-452d-bb15-5c55608467e3

Device Description

High Flow Humidifier w/Adult Cannula & 7' 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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

GMDN Terms

Code Name
35530 Heat/moisture exchanger, single-use

Identifiers

Type ID
Package 20889483074609
Primary 10889483074602

Customer Contacts

Phone
800-433-2797

Device Sizes

Type Value Unit Text
Length 7 Feet

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
General Warehouse. Do not get wet.