FDA UDI In Commercial Distribution 🇺🇸 United States

GentleMax Pro Plus

DI: 00817495022994 · Model: 7123-00-0629 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GentleMax Pro Plus
Primary DI
00817495022994
Version / Model
7123-00-0629
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-20
Public Version
2
Public Version Date
2022-10-12
Public Version Status
Update
Public Device Record Key
3bbf58dd-3951-4b66-b099-73cc5fbe845c

Device Description

ASSY, ACC HAND PIECE, MEDIUM SPOT, GMPP

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
47883 Dermatological solid-state laser system

Identifiers

Type ID
Primary 00817495022994

Customer Contacts

Phone
800-735-2737

Premarket Submissions

Submission Number Supplement Number
K201111 000