FDA UDI Not in Commercial Distribution 🇺🇸 United States

Duo-Flow®

DI: 00884908059380 · Model: XTP116MT · Medical Components, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Duo-Flow®
Primary DI
00884908059380
Version / Model
XTP116MT
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-14
Public Version
6
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8546056b-b778-4b26-aa9b-f6789a1cb500
Distribution End Date
2021-01-29

Device Description

11.5F X 15CM Duo-Flow® DOUBLE LUMEN CATHETER SET

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
37278 Double-lumen haemodialysis catheter, implantable
46979 Double-lumen haemodialysis catheter, nonimplantable

Identifiers

Type ID
Package 50884908059385
Primary 00884908059380

Customer Contacts