BEMER Therapy Systems 420200

GUDID 07640161461048

Bemer Int. AG

Hand-held deep-tissue electromagnetic stimulator
Primary Device ID07640161461048
NIH Device Record Key6dbf84ab-0a9e-4dd4-8b38-b6095e200ea7
Commercial Distribution StatusIn Commercial Distribution
Brand NameBEMER Therapy Systems
Version Model NumberB.BOX Professional
Catalog Number420200
Company DUNS448002860
Company NameBemer Int. AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
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
GS107640161461024 [Package]
Contains: 07640161462021
Package: [1 Units]
In Commercial Distribution
GS107640161461048 [Package]
Contains: 07640161462021
Package: [1 Units]
In Commercial Distribution
GS107640161462021 [Primary]

FDA Product Code

NGXStimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-05-03

On-Brand Devices [BEMER Therapy Systems]

07640161461048B.BOX Professional
07640161461017B.BOX Classic
07640161461055Professional

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