FDA UDI Not in Commercial Distribution 🇺🇸 United States

Duo-Flow®

DI: 00884908179958 · Model: MCDLT4000 · Medical Components, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Duo-Flow®
Primary DI
00884908179958
Version / Model
MCDLT4000
Catalog Number
MCDLT4000
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-04
Public Version
1
Public Version Date
2024-07-12
Public Version Status
New
Public Device Record Key
27f80716-3226-4505-be11-40717275998b
Distribution End Date
2024-07-10

Device Description

11.5F X 15CM Duo-Flow® CATHETER FULL TRAY

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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 50884908179953
Primary 00884908179958

Customer Contacts