FDA UDI In Commercial Distribution 🇺🇸 United States

PicoWay Laser System

DI: 00817495023588 · Model: 9914-CH-9060 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PicoWay Laser System
Primary DI
00817495023588
Version / Model
9914-CH-9060
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-16
Public Version
1
Public Version Date
2022-12-26
Public Version Status
New
Public Device Record Key
91584842-5c0b-4c73-960f-91be87282c25

Device Description

Picoway Laser System

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47877 Dermatological frequency-doubled solid-state laser system

Identifiers

Type ID
Primary 00817495023588

Customer Contacts

Phone
800-735-2737

Premarket Submissions

Submission Number Supplement Number
K220853 000