Identity
- Trade Name
- PM-360 FDA UDI
- Generic Name
- Transcutaneous electrical stimulation electrode, single-use FDA UDI
- Device Name
- (1) -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 FDA UDI
- Model / Reference
- PM-360 FDA UDI
- Description
- (1) -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 FDA UDI
Identifiers
- Catalog Number
- PM-360 FDA UDI
- Primary DI / UDI-DI
- 00185098000436 FDA UDI
- FDA Product Code
- IPF FDA UDI
- GMDN Term
- Transcutaneous electrical stimulation electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5850 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Transcutaneous electrical stimulation electrode, single-use
Pm-360 by Pro Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Transcutaneous electrical stimulation electrode, single-use.
- AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
- Eswallow — COMPASS HEALTH BRANDS CORP. · Class II
- TMR-ELEC-20003221 2" WH Round electrode — Emsi · Class II
- Medical Science Products — SAUVRE INTERNATIONAL, LTD. · Class II
- AdvanTrode — PEPIN MANUFACTURING, INC. · Class II
- 3x5 fabric conductive pad — BioMedical Life Systems Inc. · Class II
- MediMax Tech — MEDIMAX TECH INC. · Class II
- SuperStim Electrodes — COMPASS HEALTH BRANDS CORP. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Pro Medical Supplies, Inc.
Sources (1)
- FDA UDI a0a42f98-b3a0-45b8-939c-ce10be939c5b 35 fields · synced May 30, 2026