FDA UDI In Commercial Distribution 🇺🇸 United States

Ventlab

DI: 10889483104040 · Model: PRO-7140 · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ventlab
Primary DI
10889483104040
Version / Model
PRO-7140
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-27
Public Version
5
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
e4c8afa2-86cc-49bd-bf10-b412cb7c0bd9

Device Description

Bi-Level Circuit for Respironics Vision & Std30

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
BZD Ventilator, Non-Continuous (Respirator)

GMDN Terms

Code Name
37704 Anaesthesia breathing circuit, single-use

Identifiers

Type ID
Package 20889483104047
Primary 10889483104040

Customer Contacts

Phone
800-433-2797

Premarket Submissions

Submission Number Supplement Number
K040726 000

Storage Conditions

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