27ga OEM DEX™ Super Grip Forceps

GUDID 10817489026868

27ga OEM DEX™ Super Grip Forceps

KATALYST SURGICAL LLC

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 Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
Primary Device ID10817489026868
NIH Device Record Keyab47b719-fd4a-45bf-a88f-f9e6701c2984
Commercial Distribution Discontinuation2023-04-25
Commercial Distribution StatusNot in Commercial Distribution
Brand Name27ga OEM DEX™ Super Grip Forceps
Version Model NumberDVFO4034-27
Company DUNS007883297
Company NameKATALYST SURGICAL LLC
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 Datetrue
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
GS100817489026861 [Unit of Use]
GS110817489026868 [Primary]

FDA Product Code

HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-04-27
Device Publish Date2017-12-19

Devices Manufactured by KATALYST SURGICAL LLC

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