Disposable Microforceps: End-gripping.(20 gauge / 0.9 mm) 1286.BD

GUDID 18717872004706

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

Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
Primary Device ID18717872004706
NIH Device Record Keya97ea2d7-e6cb-439a-91c2-845b68d140c9
Commercial Distribution StatusIn Commercial Distribution
Brand NameDisposable Microforceps: End-gripping.(20 gauge / 0.9 mm)
Version Model Number1286.BD
Catalog Number1286.BD
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
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS108717872004709 [Primary]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]
GS118717872004706 [Unit of Use]

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 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 [Disposable Microforceps: End-gripping.(20 gauge / 0.9 mm)]

187178720047131286.BD
187178720047061286.BD

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