FDA UDI In Commercial Distribution 🇺🇸 United States

DUO-VENT

DI: 00085412079691 · Model: ACT5439 · BAXTER INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DUO-VENT
Primary DI
00085412079691
Version / Model
ACT5439
Catalog Number
ACT5439
Company Name
BAXTER INTERNATIONAL INC.
Labeler DUNS
005146311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
c4b64771-5c9a-445c-8042-a68c0e909b98

Device Description

Solution Set with DUO-VENT Spike, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 50085412079696
Primary 00085412079691

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142011 000