Titanium Schepens Forked Retractor

GUDID 00817489029381

KATALYST SURGICAL LLC

Ocular hook/spatula/manipulator, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable

Primary Device ID	00817489029381
NIH Device Record Key	3d967e56-a813-4fc9-a74f-2c24541fb057
Commercial Distribution Status	In Commercial Distribution
Brand Name	Titanium Schepens Forked Retractor
Version Model Number	2012
Company DUNS	007883297
Company Name	KATALYST SURGICAL LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817489029381 [Primary]

FDA Product Code

HNQ	Hook, Ophthalmic