FDA UDI In Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608020010 · Model: PMIS2023 · PROGRESSIVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMI
Primary DI
00812608020010
Version / Model
PMIS2023
Catalog Number
PMIS2023
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2022-04-04
Public Version Status
Update
Public Device Record Key
d8f63473-883a-4545-b6e4-81852812e33c

Device Description

PMI Straight Huber Needle w/Female Luer Connector 20G x 2 ¾"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
17180 Subcutaneous infusion/injection port needle

Identifiers

Type ID
Package 10812608020017
Primary 00812608020010

Customer Contacts

Phone
314-961-5786