EDINTRAK 4058-6

GUDID 37613327364232

Hook Blade

Stryker Trauma SA

Scalpel blade, single-use
Primary Device ID37613327364232
NIH Device Record Keybabde4cb-b9c4-4fcb-81a2-b8adc311c651
Commercial Distribution StatusIn Commercial Distribution
Brand NameEDINTRAK
Version Model Number4058-6
Catalog Number4058-6
Company DUNS481999654
Company NameStryker Trauma SA
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
GS107613327364231 [Primary]
GS137613327364232 [Package]
Contains: 07613327364231
Package: pack [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-11-28

On-Brand Devices [EDINTRAK]

37613327364300Hook Blade
07613327364255Hook Blade
37613327364232Hook Blade
07613327364200Hook Blade
07613327363265Metatarsal Spreader
07613327363180System
07613327363159Micro Elevator
07613327362855Obturator
07613327362848Probe
07613327362831System
07613327362770Micro Blade Handle
07613327362749Cannula
07613327362725Sterilization Tray
07613327362688Obturator
07613327362602Micro Hook Blade
07613327362589Cannula
07613327362480Angled Micro Hook Blade
37613327362214Micro Tip Swabs

Trademark Results [EDINTRAK]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EDINTRAK
EDINTRAK
74618042 1986326 Live/Registered
HOWMEDICA OSTEONICS CORP
1995-01-05

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.