FDA UDI In Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608021833 · Model: PMIFR200 · PROGRESSIVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMI
Primary DI
00812608021833
Version / Model
PMIFR200
Catalog Number
PMIFR200
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-31
Public Version
1
Public Version Date
2018-07-02
Public Version Status
New
Public Device Record Key
34aa2d82-2523-423d-8147-c45b95b156af

Device Description

PMI IV admin set with flow regulator and needle-free y-site approx. 11" from distal end, 100" length, 20 drop, 15 micron filter in drip chamber, rotating male luer lock, vented cap, pinch clamp

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
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
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 00812608021840
Primary 00812608021833

Customer Contacts

Phone
314-961-5786