FDA UDI In Commercial Distribution 🇺🇸 United States

FINESSE REFLEX™

DI: 07612717072152 · Model: 805.88L · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
FINESSE REFLEX™
Primary DI
07612717072152
Version / Model
805.88L
Catalog Number
805.88L
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-02
Public Version
1
Public Version Date
2025-12-10
Public Version Status
New
Public Device Record Key
e44358c1-ccbc-4689-9e23-45106601fd4f

Device Description

25+™ SHARKSKIN™ ILM Forceps REFLEX - Long

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
HNR Forceps, ophthalmic

GMDN Terms

Code Name
62478 Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

Identifiers

Type ID
Package 17612717072159
Primary 07612717072152

Device Sizes

Type Value Unit Text
Needle Gauge 25 Gauge
Device Size Text, specify Long