FDA UDI In Commercial Distribution 🇺🇸 United States

FK20210E

DI: 00850005864141 · Model: FK20210E · PATHEN MEDICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FK20210E
Primary DI
00850005864141
Version / Model
FK20210E
Company Name
PATHEN MEDICAL LLC
Labeler DUNS
042928915
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-28
Public Version
1
Public Version Date
2019-04-05
Public Version Status
New
Public Device Record Key
eb88932f-8c17-4ad4-8522-1ac74fef2db4

Device Description

5” (13cm) Bi-fuse Minibore extension set with 3 slide clamps male luer lock and 2 non-bonded needle-free connectors

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 10850005864148
Primary 00850005864141

Customer Contacts

Phone
8773185421