FDA UDI In Commercial Distribution 🇺🇸 United States

Kit, 785 HP and DG

DI: 00817495022680 · Model: 7123-00-0245 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kit, 785 HP and DG
Primary DI
00817495022680
Version / Model
7123-00-0245
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-26
Public Version
9
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
e568aad2-b1e4-4f1c-b570-d3304082d057

Device Description

Handpiece Assembly

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
Yes
Has Expiration Date
No
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
65509 Dermatological laser beam producing handpiece

Identifiers

Type ID
Primary 00817495022680

Premarket Submissions

Submission Number Supplement Number
K220853 000