Forceps for removal 23 gauge/0.6 mm cannula with closure valve. 1276.2

GUDID 08717872003092

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

Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Primary Device ID08717872003092
NIH Device Record Key995a4c10-b40b-42b9-95b1-2ddbcb1a941b
Commercial Distribution StatusIn Commercial Distribution
Brand NameForceps for removal 23 gauge/0.6 mm cannula with closure valve.
Version Model Number1276.2
Catalog Number1276.2
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
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]
GS108717872003092 [Primary]

FDA Product Code

HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic
HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


[08717872003092]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-22
Device Publish Date2021-02-01

On-Brand Devices [Forceps for removal 23 gauge/0.6 mm cannula with closure valve.]

087178720031081276.2
087178720030921276.2

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.