FDA UDI In Commercial Distribution 🇺🇸 United States

PMGF090NY

DI: 00850005864417 · Model: PMGF090NY · PATHEN MEDICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMGF090NY
Primary DI
00850005864417
Version / Model
PMGF090NY
Company Name
PATHEN MEDICAL LLC
Labeler DUNS
042928915
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-15
Public Version
1
Public Version Date
2019-07-23
Public Version Status
New
Public Device Record Key
38f60fe5-5db3-4ab9-bd14-501dfe2a1861

Device Description

90" Flow regulator, 1 needle free Y site, 8" above distal tip, pinch clamp,.22 micron filter, male spin luer lock

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 10850005864414
Primary 00850005864417

Customer Contacts

Phone
8773185421