Large replacement backflush Reservoir for 1281.C. 1281.C1

GUDID 18717872003846

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 ID18717872003846
NIH Device Record Key028e7767-d567-4f6a-ac8d-67830ceb1f5c
Commercial Distribution StatusIn Commercial Distribution
Brand NameLarge replacement backflush Reservoir for 1281.C.
Version Model Number1281.C1
Catalog Number1281.C1
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count10
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
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS108717872003849 [Primary]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]
GS118717872003846 [Unit of Use]

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

[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


[18717872003846]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-22
Device Publish Date2021-02-09

On-Brand Devices [Large replacement backflush Reservoir for 1281.C.]

187178720160991281.C1
187178720038461281.C1

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