FDA UDI In Commercial Distribution 🇺🇸 United States

VOYAGER

DI: 00814112020296 · Model: 5170-0000 · CARDIACASSIST, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VOYAGER
Primary DI
00814112020296
Version / Model
5170-0000
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-17
Public Version
3
Public Version Date
2018-10-03
Public Version Status
Update
Public Device Record Key
bfa2c4ac-a931-48d1-a2c9-df3ea68008e9

Device Description

Voyager Securement Kit for Blood Pump and Oxygenator

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KRI Accessory Equipment, Cardiopulmonary Bypass

GMDN Terms

Code Name
36373 Cardiopulmonary bypass system mounting unit

Identifiers

Type ID
Primary 00814112020296

Customer Contacts

Phone
+14129637770