Kusaka Scleral Depressor. 1040

GUDID 08717872017266

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

Orbital depressor, reusable
Primary Device ID08717872017266
NIH Device Record Key5470f3c1-6560-42e5-8e4f-e520e92a1573
Commercial Distribution StatusIn Commercial Distribution
Brand NameKusaka Scleral Depressor.
Version Model Number1040
Catalog Number1040
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count1
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
GS108717872017266 [Primary]

FDA Product Code

HNXDepressor, Orbital

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


[08717872017266]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-08-05
Device Publish Date2020-11-16

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