Scharioth IOL Scleral fixation forceps, straight & curved. (25 gauge / 0.5mm) 1286.SFD

GUDID 08717872017839

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 ID08717872017839
NIH Device Record Keyd52de7b6-0e03-4d23-91e7-86964c4b49e6
Commercial Distribution StatusIn Commercial Distribution
Brand NameScharioth IOL Scleral fixation forceps, straight & curved. (25 gauge / 0.5mm)
Version Model Number1286.SFD
Catalog Number1286.SFD
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 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
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [Primary]
GS108717872017839 [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 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 [Scharioth IOL Scleral fixation forceps, straight & curved. (25 gauge / 0.5mm)]

087178720060861286.SFD
087178720178391286.SFD

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