FINESSE REFLEX™ 805.88L

GUDID 17612717072159

Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

Primary Device ID	17612717072159
NIH Device Record Key	e44358c1-ccbc-4689-9e23-45106601fd4f
Commercial Distribution Status	In Commercial Distribution
Brand Name	FINESSE REFLEX™
Version Model Number	805.88L
Catalog Number	805.88L
Company DUNS	008018525
Company Name	Alcon Laboratories, Inc.
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	07612717072152 [Primary]
GS1	17612717072159 [Package] Contains: 07612717072152 Package: BX [6 Units] In Commercial Distribution

HNR	Forceps, ophthalmic

Steralize Prior To Use	false
Device Is Sterile	true

17612717072159	25+™ SHARKSKIN™ ILM Forceps REFLEX - Long
17612717072135	25+™ Endgrasping Forceps REFLEX - Long
17612717072128	25+™ GRIESHABER MAXGrip™ Forceps REFLEX - Long

Mark Image Registration \| Serial	Company Trademark Application Date
FINESSE REFLEX 87721049 not registered Live/Pending	Novartis AG 2017-12-14