Myo Plus trial kit

GUDID 04064411245340

Otto Bock Healthcare Products GmbH

Myoelectric hand prosthesis
Primary Device ID04064411245340
NIH Device Record Key65d4e7f7-5e7b-4ec0-a22b-4bd3a7f583e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameMyo Plus trial kit
Version Model Number642V64=T-PLUS-OB
Company DUNS300802068
Company NameOtto Bock Healthcare Products GmbH
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-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104064411245340 [Primary]

FDA Product Code

GXYElectrode, Cutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-27
Device Publish Date2020-03-19

On-Brand Devices [Myo Plus trial kit]

04032767949199642V64=T-PLUS-S
04032767946761642V64=T-PLUS-OB
04064411245357642V64=T-PLUS-S
04064411245340642V64=T-PLUS-OB

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