Meridian Perforator PER C6-9-S

GUDID EADEPERC69S1

adeor Medical AG

Automatic cranial perforator, single-use
Primary Device IDEADEPERC69S1
NIH Device Record Keya357d8d2-f0f6-48e1-b2c7-eaa21f8202f3
Commercial Distribution StatusIn Commercial Distribution
Brand NameMeridian Perforator
Version Model NumberClassic
Catalog NumberPER C6-9-S
Company DUNS341188943
Company Nameadeor Medical 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 Usetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEADEPERC69S1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HBFDrills, Burrs, Trephines & Accessories (Compound, Powered)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-22
Device Publish Date2017-02-11

On-Brand Devices [Meridian Perforator]

EADEPERC811S1Classic
EADEPERC69S1Classic
EADEPERC1114S1Classic
EADEPER711SP1alpha
EADEPER711S1alpha
EADEPER1114SP1alpha
EADEPER1114SG1alpha
EADEPER1114S1alpha

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