Closure valves for 23 gauge/0.6 mm vitrectomy system. 1272.ERPP6

GUDID 18717872002535

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

Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use
Primary Device ID18717872002535
NIH Device Record Key01963294-e769-417b-9256-f5bffb5cc138
Commercial Distribution StatusIn Commercial Distribution
Brand NameClosure valves for 23 gauge/0.6 mm vitrectomy system.
Version Model Number1272.ERPP6
Catalog Number1272.ERPP6
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count4
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
GS108717872002538 [Primary]
GS118717872002535 [Unit of Use]

FDA Product Code

NGYCannula, Trocar, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-09
Device Publish Date2021-02-01

On-Brand Devices [Closure valves for 23 gauge/0.6 mm vitrectomy system.]

187178720025351272.ERPP6
187178720025281272.ERPP6

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