Backflush Instrument with 20G / 0.9 mm blunt needle 1281.A

GUDID 08717872003382

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 ID08717872003382
NIH Device Record Key5966caea-7a77-4b1e-bbb1-1e5744a8d061
Commercial Distribution StatusIn Commercial Distribution
Brand NameBackflush Instrument with 20G / 0.9 mm blunt needle
Version Model Number1281.A
Catalog Number1281.A
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
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]
GS108717872003382 [Primary]

FDA Product Code

GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable
GDMNeedle, Aspiration And Injection, Reusable

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


[08717872003382]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-22
Device Publish Date2020-11-16

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18717872026135 - Backflush Instrument with 23 gauge / 0.6 mm brush needle and active aspiration.2021-02-24
18717872026142 - Backflush Instrument with 20 gauge / 0.9 mm brush needle.2021-02-24
18717872026159 - Backflush Instrument with 20 gauge / 0.9 mm blunt needle.2021-02-24

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