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Hyper Jet

FDA UDI

Class I (US FDA UDI)

by Eunsung Global Corp

Identity

Trade Name
HYPER JET FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Device Name
While vibrating at a high speed, the microtips of this device apply physical stimulation to the facial skin to facilitate active ingredients to penetrate in the skin. FDA UDI
Model / Reference
ESK-2162HJ FDA UDI
Description
While vibrating at a high speed, the microtips of this device apply physical stimulation to the facial skin to facilitate active ingredients to penetrate in the skin. FDA UDI

Identifiers

Primary DI / UDI-DI
08800060501668 FDA UDI
FDA Product Code
GFE FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

Hyper Jet by Eunsung Global Corp — Class I — 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
Eunsung Global Corp

Sources (1)

  • FDA UDI 77afd555-23d5-4e1a-a2c4-bf605cc3b1e5 33 fields · synced Jun 8, 2026