Microforceps: Serrated Jaws.(23 gauge / 0.6 mm) 1286.C06

GUDID 08717872004846

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

Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
Primary Device ID08717872004846
NIH Device Record Keye898a934-905b-4a6c-8ace-c868fd5c95bd
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicroforceps: Serrated Jaws.(23 gauge / 0.6 mm)
Version Model Number1286.C06
Catalog Number1286.C06
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
GS108717872004846 [Primary]

FDA Product Code

HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


[08717872004846]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-17
Device Publish Date2021-02-09

On-Brand Devices [Microforceps: Serrated Jaws.(23 gauge / 0.6 mm)]

087178720048461286.C06
087178720048391286.C06

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