Backflush instrument with active aspiration 20G / 0.9 mm. 1281.T

GUDID 08717872003979

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Primary Device ID08717872003979
NIH Device Record Keydf216c3d-c769-409b-8c68-91878913712e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBackflush instrument with active aspiration 20G / 0.9 mm.
Version Model Number1281.T
Catalog Number1281.T
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
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 Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]
GS108717872003979 [Primary]

FDA Product Code

HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


[08717872003979]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-22
Device Publish Date2021-02-02

On-Brand Devices [Backflush instrument with active aspiration 20G / 0.9 mm.]

087178720039861281.T
087178720039791281.T

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