FDA UDI In Commercial Distribution 🇺🇸 United States

OPTIMIS FUSION

DI: 03700542625460 · Model: OPTIMIS FUSION · QUANTEL MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OPTIMIS FUSION
Primary DI
03700542625460
Version / Model
OPTIMIS FUSION
Company Name
QUANTEL MEDICAL
Labeler DUNS
738574953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b15e56ab-63a1-461c-bd23-a0a6a41ce17c

Device Description

SLT/YAG Laser (Dual-mode laser cavity, 532nm and 1064nm)

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HQF Laser, Ophthalmic

GMDN Terms

Code Name
16947 Ophthalmic solid-state laser system, photodisruption

Identifiers

Type ID
Primary 03700542625460

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140336 000