MVR Blade 23-G, angled 1282.D06

GUDID 18717872004072

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

Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use
Primary Device ID18717872004072
NIH Device Record Key826606ec-ae2c-47e5-9c1a-16ec832c40c1
Commercial Distribution StatusIn Commercial Distribution
Brand NameMVR Blade 23-G, angled
Version Model Number1282.D06
Catalog Number1282.D06
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count6
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
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS108717872004075 [Primary]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]
GS118717872004072 [Unit of Use]

FDA Product Code

HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, Ophthalmic
HNNKnife, 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 Date2021-02-09

On-Brand Devices [MVR Blade 23-G, angled]

187178720040891282.D06
187178720040721282.D06

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