FDA UDI In Commercial Distribution 🇺🇸 United States

Ventlab

DI: 10889483231739 · Model: ST710 · VENTLAB, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ventlab
Primary DI
10889483231739
Version / Model
ST710
Catalog Number
ST710
Company Name
VENTLAB, LLC
Labeler DUNS
038305402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-18
Public Version
1
Public Version Date
2023-07-26
Public Version Status
New
Public Device Record Key
66ed2073-0c90-4e70-9aa4-798e08e12781

Device Description

T-Piece Resuscitator with 7ft O2 tubing, Xtra Small Neonate mask & Pop-off Override

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 Unsafe
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
BTL Ventilator, emergency, powered (resuscitator)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Primary 10889483231739

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173373 000