FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-FUSE®

DI: 00884908147483 · Model: MRPP96AFS · Medical Components, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRO-FUSE®
Primary DI
00884908147483
Version / Model
MRPP96AFS
Catalog Number
MRPP96AFS
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-08
Public Version
1
Public Version Date
2019-11-18
Public Version Status
New
Public Device Record Key
36dae05a-b93a-488a-9bdd-8f35c1c024d2

Device Description

9.6F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLECT PORT W/AT SILICONE CATHETERSILICONE CATHET

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 50884908147488
Primary 00884908147483

Customer Contacts