FDA UDI In Commercial Distribution 🇺🇸 United States

primeMIDLINE

DI: 00813623010154 · Model: PFM3SML20N · PFM MEDICAL INCORPORATED
Product Codes
1
GMDN Terms
2
Identifiers
3
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
primeMIDLINE
Primary DI
00813623010154
Version / Model
PFM3SML20N
Catalog Number
PFM3SML20N
Company Name
PFM MEDICAL INCORPORATED
Labeler DUNS
097736867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-31
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
e30c899c-96b5-4aa7-9078-5893d164ccbe

Device Description

3F x 20cm Single Lumen CT Midline

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
PND Midline Catheter

GMDN Terms

Code Name
40601 Peripheral vascular catheter
61594 Central venous catheterization kit, short-term

Identifiers

Type ID
Package 20813623010158
Package 10813623010151
Primary 00813623010154

Customer Contacts

Phone
7607588749

Premarket Submissions

Submission Number Supplement Number
K173114 000