Titanium Jaffe-Knolle Iris Hook, Angled

GUDID 00817489029275

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	00817489029275
NIH Device Record Key	f46b938b-7cb0-4ff3-bb50-2756b39d5ebb
Commercial Distribution Status	In Commercial Distribution
Brand Name	Titanium Jaffe-Knolle Iris Hook, Angled
Version Model Number	2003A
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	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817489029275 [Primary]

FDA Product Code

HNQ	Hook, Ophthalmic