Revive PRO IR

GUDID EJKP100003973A0

JK-Products GmbH

Vibration platform exerciser, stationary
Primary Device IDEJKP100003973A0
NIH Device Record Keye641442a-86d0-443c-8f7a-6253ba50920d
Commercial Distribution StatusIn Commercial Distribution
Brand NameRevive PRO IR
Version Model NumberJK 194/RV32-10 VBR
Company DUNS316232073
Company NameJK-Products GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEJKP100003973A0 [Primary]

FDA Product Code

BXBExerciser, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-23
Device Publish Date2023-11-15

Devices Manufactured by JK-Products GmbH

EJKP100004042A0 - Ergoline Vitality Pure Light 3 (10 min)2024-03-07
EJKP100003952B0 - Revive2023-12-11
EJKP100003960B0 - Revive RVT302023-12-11
EJKP100003973A0 - Revive PRO IR2023-11-23
EJKP100003973A0 - Revive PRO IR2023-11-23
EJKP100003892A0 - VITALITY 46/3 PLT AC USA2023-06-08
EJKP100003946A0 - Ergoline/PASSION PLUS 40/3 Smart Performance2023-06-08
EJKP100003952A0 - Revive 7200 2023-06-08
EJKP100003960A0 - Revive RVT302023-05-08

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