FDA UDI In Commercial Distribution 🇺🇸 United States

PM-360

DI: 10185098000433 · Model: PM-360 · PRO MEDICAL SUPPLIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
PM-360
Primary DI
10185098000433
Version / Model
PM-360
Catalog Number
PM-360
Company Name
PRO MEDICAL SUPPLIES, INC.
Labeler DUNS
135741127
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-08-24
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
7896015a-d383-4aff-b0ad-fb1d470c1b44

Device Description

(30) Per Case -Transcutaneous Nerve Stimulator -Five Mode with Timer, Dual Channel 4 Leads - Zipper Case Includes: device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 10185098000433
Unit of Use 18509800043630

Customer Contacts

Phone
215-938-0200