Replacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpie 1281.A5D06

GUDID 18717872003518

Replacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpiece

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

Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula
Primary Device ID18717872003518
NIH Device Record Keyae183da0-5f76-46c1-b6c1-4bf7352b81c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameReplacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpie
Version Model Number1281.A5D06
Catalog Number1281.A5D06
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 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
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS108717872003511 [Primary]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]
GS118717872003518 [Unit of Use]

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 Usefalse
Device Is Steriletrue

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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18717872018567 - Disposable Microscissors: Hooked. (27 gauge / 0.4 mm)2021-02-24
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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