Titanium Katzen LASIK Flap Unzipper

GUDID 00840096207361

Titanium Katzen LASIK Flap Unzipper

KATALYST SURGICAL LLC

Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable Ocular hook/spatula/manipulator, reusable
Primary Device ID00840096207361
NIH Device Record Keyf92892de-5020-4134-9932-7ff07d0d5570
Commercial Distribution StatusIn Commercial Distribution
Brand NameTitanium Katzen LASIK Flap Unzipper
Version Model Number8090
Company DUNS007883297
Company NameKATALYST SURGICAL LLC
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]
GS100840096207361 [Primary]

FDA Product Code

HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic
HNQHook, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


[00840096207361]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-26
Device Publish Date2020-05-18

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