23ga Slim DEX™ EZPeel Forceps

GUDID 00840096212938

23ga Slim DEX™ EZPeel 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
Primary Device ID00840096212938
NIH Device Record Key3944933c-ea7a-4046-9d15-51007fd6fafd
Commercial Distribution StatusIn Commercial Distribution
Brand Name23ga Slim DEX™ EZPeel Forceps
Version Model NumberDVFO4037-23
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 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
GS100840096212938 [Unit of Use]
GS110840096212935 [Primary]

FDA Product Code

HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-14
Device Publish Date2020-07-06

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