FDA UDI In Commercial Distribution 🇺🇸 United States

FINESSE ModifEYE

DI: 07612717072077 · Model: 337.68 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FINESSE ModifEYE
Primary DI
07612717072077
Version / Model
337.68
Catalog Number
337.68
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-25
Public Version
1
Public Version Date
2024-10-03
Public Version Status
New
Public Device Record Key
f6064c53-eab9-4bf0-bec5-a4bc75479ee7

Device Description

27+ ModifEYE Soft Tip Backflush

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
47130 Vitrectomy fluid/gas handling handpiece/cannula

Identifiers

Type ID
Package 17612717072074
Primary 07612717072077

Device Sizes

Type Value Unit Text
Needle Gauge 27 Gauge