FINESSE ModifEYE 337.64

GUDID 17612717072067

25G ModifEYE Soft Tip Backflush

Alcon Laboratories, Inc.

Vitrectomy fluid/gas handling handpiece/cannula
Primary Device ID17612717072067
NIH Device Record Keye07cb15d-644d-4a5a-b6d7-ec72b9153ed0
Commercial Distribution StatusIn Commercial Distribution
Brand NameFINESSE ModifEYE
Version Model Number337.64
Catalog Number337.64
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge
Needle Gauge25 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS107612717072060 [Primary]
GS117612717072067 [Package]
Contains: 07612717072060
Package: Box [6 Units]
In Commercial Distribution

FDA Product Code

HMXCannula, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-03
Device Publish Date2024-09-25

On-Brand Devices [FINESSE ModifEYE]

1761271707207427+ ModifEYE Soft Tip Backflush
1761271707206725G ModifEYE Soft Tip Backflush
1761271707210427+ ModifEYE Soft Tip Backflush - Long
1761271707209825G ModifEYE Soft Tip Backflush - Long

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