Lamination pattern for outer socket

GUDID 04032767159970

Otto Bock Healthcare Products GmbH

Myoelectric hand prosthesis
Primary Device ID04032767159970
NIH Device Record Keyf11ad6e0-6551-44e0-9a5a-e791ac309a8e
Commercial Distribution Discontinuation2020-03-18
Commercial Distribution StatusNot in Commercial Distribution
Brand NameLamination pattern for outer socket
Version Model Number13E192
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 Batchtrue
Serial Numberfalse
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
GS104032767159970 [Primary]

FDA Product Code

GXYElectrode, Cutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-03-19
Device Publish Date2016-09-23

On-Brand Devices [Lamination pattern for outer socket]

0403276725391313E204
0403276715997013E192

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