FDA UDI In Commercial Distribution 🇺🇸 United States

Catheter w/ Blunt Introducer

DI: 10816203022100 · Model: VV23F · ORIGEN BIOMEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Catheter w/ Blunt Introducer
Primary DI
10816203022100
Version / Model
VV23F
Company Name
ORIGEN BIOMEDICAL, INC.
Labeler DUNS
625272232
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
818891c6-4a0f-407a-a572-3c5cad4d076a

Device Description

ECMO Reinforced Dual Lumen Cannula, 23F

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
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

GMDN Terms

Code Name
58726 Mobile extracorporeal gas exchange system catheter kit

Identifiers

Type ID
Primary 10816203022100

Customer Contacts

Phone
512-474-7278