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Awq-104l

FDA UDI

Class II (US FDA UDI)

by Tens Plus Industrial Company

Identity

Trade Name
AWQ-104L FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Device Name
The AWQ-104L w L-Digital Meter is the latest improved version of the multipurpose WQ-10 electro-therapy series from China, now with 4 outputs and large 0.5" x 0.9" LCD digital meter. The AWQ-104L is able to display and fine tune frequency selection through two separate ranges: 1 to 100 Hz (low) and 10 to 1,000 Hz (High). Unit also features: 4 independently controlled output channels which provide stimulation to 8 needles, polarity reversal [i.e. tonification (+) and sedation (-)] switches for each channel, Hi/Low voltage switch, and 2 frequency ranges (X1, X10). New integrated circuitry assures no interference or crossover. The AWQ-104L is also capable of delivering micro-current when the intensity is set just below the sensorial threshold level. Powered by 9 volt battery. Three adjustable pulse modes are also offered: continuous, intermittent (discontinuous), and dense-disperse. Accessories include 5" long pen shaped treatment probe with hand ground pole and wire, 4 sets of alligator clip wires, sturdy carrying case, 9-volt battery, and instructions. 1-year warranty from date of purchase. FDA UDI
Model / Reference
ED3923 FDA UDI
Description
The AWQ-104L w L-Digital Meter is the latest improved version of the multipurpose WQ-10 electro-therapy series from China, now with 4 outputs and large 0.5" x 0.9" LCD digital meter. The AWQ-104L is able to display and fine tune frequency selection through two separate ranges: 1 to 100 Hz (low) and 10 to 1,000 Hz (High). Unit also features: 4 independently controlled output channels which provide stimulation to 8 needles, polarity reversal [i.e. tonification (+) and sedation (-)] switches for each channel, Hi/Low voltage switch, and 2 frequency ranges (X1, X10). New integrated circuitry assures no interference or crossover. The AWQ-104L is also capable of delivering micro-current when the intensity is set just below the sensorial threshold level. Powered by 9 volt battery. Three adjustable pulse modes are also offered: continuous, intermittent (discontinuous), and dense-disperse. Accessories include 5" long pen shaped treatment probe with hand ground pole and wire, 4 sets of alligator clip wires, sturdy carrying case, 9-volt battery, and instructions. 1-year warranty from date of purchase. FDA UDI

Identifiers

Catalog Number
ED3923 FDA UDI
Primary DI / UDI-DI
14897076720016 FDA UDI
510(k) Number
K050989 FDA UDI
FDA Product Code
GZJ FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

Awq-104l by Tens Plus Industrial Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analgesic transcutaneous electrical nerve stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tens Plus Industrial Company

Sources (1)

  • FDA UDI a45fca27-17d6-42fc-8443-e1aa05bf84fc 36 fields · synced May 31, 2026