Extendible curved spatula. (23 gauge / 0.6 mm) 1290.ECS06

GUDID 18717872017829

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

Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use
Primary Device ID18717872017829
NIH Device Record Keyeef40a9e-5ff4-4c00-87db-f7d1a7545662
Commercial Distribution StatusIn Commercial Distribution
Brand NameExtendible curved spatula. (23 gauge / 0.6 mm)
Version Model Number1290.ECS06
Catalog Number1290.ECS06
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count5
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
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS108717872017822 [Primary]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]
GS118717872017829 [Unit of Use]

FDA Product Code

HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, Ophthalmic
HNDSpatula, 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 Date2021-02-11

On-Brand Devices [Extendible curved spatula. (23 gauge / 0.6 mm)]

187178720064341290.ECS06
187178720178291290.ECS06

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