Activator AC

GUDID E22193001

VOCO GmbH

Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use Dental material injection cannula, single-use
Primary Device IDE22193001
NIH Device Record Key24be238a-9ec0-48eb-b063-f3248426611d
Commercial Distribution StatusIn Commercial Distribution
Brand NameActivator AC
Version Model Number9300
Company DUNS316699578
Company NameVOCO 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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx
Phone999-999-9999
Emailxxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE22193001 [Primary]

FDA Product Code

EJBHandle, Instrument, Dental

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-08-21
Device Publish Date2019-05-03

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