FDA UDI In Commercial Distribution 🇺🇸 United States

Pro-Fuse® CT Port

DI: 00884908109719 · Model: MRPP96AFS · Medical Components, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Fuse® CT Port
Primary DI
00884908109719
Version / Model
MRPP96AFS
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
5
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
282076a0-0bbf-43a7-9421-428f55915b0d

Device Description

9.6F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLE SILICONE CATHETER

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
MR Conditional
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
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
61494 Vascular port/catheter

Identifiers

Type ID
Package 50884908109714
Primary 00884908109719

Customer Contacts