FDA UDI In Commercial Distribution 🇺🇸 United States

Alcon

DI: 00380657515882 · Model: 8065751588 · Alcon Laboratories, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Alcon
Primary DI
00380657515882
Version / Model
8065751588
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b8cf72df-103f-4622-a426-e528ae61dd1d

Device Description

23 GA Illuminated Flexible Curved Laser Probe

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HQF Laser, ophthalmic
HQE Instrument, vitreous aspiration and cutting, ac-powered
HQB Photocoagulator and accessories

GMDN Terms

Code Name
61162 Ophthalmic laser system beam guide

Identifiers

Type ID
Package 10380657515889
Primary 00380657515882

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 23 Gauge