D-ACTOR®

GUDID 07630039100407

Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.

Storz Medical AG

Electric massager
Primary Device ID07630039100407
NIH Device Record Keybd9dda2c-a93a-4118-b8f0-55fc30b0f56b
Commercial Distribution StatusIn Commercial Distribution
Brand NameD-ACTOR®
Version Model Number100 silver [000x]
Company DUNS481967776
Company NameStorz Medical AG
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-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107630039100407 [Primary]

FDA Product Code

ISAMassager, Therapeutic, Electric

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-01-23
Device Publish Date2016-08-24

On-Brand Devices [D-ACTOR®]

07630039101121Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.
07630039101060Pulse Activation Therapy System
07630039101039200
07630039100476Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.
07630039100414Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.
07630039100407Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.
07630039100391Equipment for the extracorporeal pneumatically operated ballistic pressure wave therapy.

Trademark Results [D-ACTOR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
D-ACTOR
D-ACTOR
78637008 3415689 Live/Registered
Storz Medical AG
2005-05-25

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