← Back to catalogue

Ergoline/ SUNRISE 480 Turbo Power + Vibra Shape

FDA UDI

Class II (US FDA UDI)

by JK-Products GmbH

Identity

Trade Name
Ergoline/ SUNRISE 480 Turbo Power + Vibra Shape FDA UDI
Generic Name
Vibration platform exerciser, stationary FDA UDI
Model / Reference
JK 98 / 48-0 FDA UDI

Identifiers

Primary DI / UDI-DI
EJKP100003333A0 FDA UDI
FDA Product Code
LEJ FDA UDI
BXB FDA UDI
GMDN Term
Vibration platform exerciser, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4635 FDA UDI
890.5380 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

Yes

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

Yes

FDA UDI

Category: Ultraviolet tanning deviceVibration platform exerciser, stationary

Ergoline/ SUNRISE 480 Turbo Power + Vibra Shape by JK-Products GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vibration platform exerciser, stationary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
JK-Products GmbH

Sources (1)

  • FDA UDI ed84992f-0cbf-4ec6-849f-fa6c97d8a9e2 32 fields · synced May 31, 2026