270104

GUDID 10886705013807

Knot Pusher 1.5mm

Medos International Sàrl

Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable
Primary Device ID10886705013807
NIH Device Record Key378816e5-b0c8-4176-a5c5-ba9ec593f96f
Commercial Distribution StatusIn Commercial Distribution
Version Model Number270104
Catalog Number270104
Company DUNS482661753
Company NameMedos International Sàrl
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110886705013807 [Primary]

FDA Product Code

NBHACCESSORIES,ARTHROSCOPIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


[10886705013807]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2024-03-18
Device Publish Date2015-09-01

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10705034507828 - VIPER PRIME2024-04-11 VIPER PRIME NAVIGATION STYLET
10886705012367 - COR2024-03-27 COR Disposable Kit, 6mm
10886705012374 - COR2024-03-27 COR Disposable Kit, 8mm
10886705012381 - COR2024-03-27 COR Disposable Kit, 10mm
10886705012404 - COR2024-03-27 COR Disposable Kit, 8mm w/Perpendicularity
10886705012398 - COR2024-03-18 COR Disposable Kit, 6mm w/Perpendicularity
10886705012411 - COR2024-03-18 COR Disposable Kit, 10mm w/Perpendicularity

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