FDA UDI In Commercial Distribution 🇺🇸 United States

T-Port

DI: 07640110987247 · Model: 616.365.2080-A · PFM MEDICAL INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
T-Port
Primary DI
07640110987247
Version / Model
616.365.2080-A
Company Name
PFM MEDICAL INCORPORATED
Labeler DUNS
097736867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-27
Public Version
1
Public Version Date
2020-03-06
Public Version Status
New
Public Device Record Key
1e43e126-f8fe-43b8-9163-70a75e65271e

Device Description

T-Port PUR Kit HF with 8F x 750 mm Attachable Polyurethane 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
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
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

GMDN Terms

Code Name
61494 Vascular port/catheter

Identifiers

Type ID
Package 07640110981597
Primary 07640110987247

Customer Contacts

Phone
7607588749

Premarket Submissions

Submission Number Supplement Number
K073210 000