FDA UDI In Commercial Distribution 🇺🇸 United States

DUO-FLOW®

DI: 00884908143102 · Model: DXTP119MT · Medical Components, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DUO-FLOW®
Primary DI
00884908143102
Version / Model
DXTP119MT
Catalog Number
DXTP119MT
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-25
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
548bfb1a-a1a5-4615-b058-c242a022a39d

Device Description

11.5F X 24CM DUO-FLOW® DOUBLE LUMEN CATHETER SETDOUBLE

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNZ Accessories, a-v shunt

GMDN Terms

Code Name
46979 Double-lumen haemodialysis catheter, nonimplantable

Identifiers

Type ID
Package 50884908143107
Primary 00884908143102

Customer Contacts