FDA UDI In Commercial Distribution 🇺🇸 United States

Pro Delivery System, Refurbished

DI: 00817495024592 · Model: FIN100985 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pro Delivery System, Refurbished
Primary DI
00817495024592
Version / Model
FIN100985
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-01
Public Version
1
Public Version Date
2023-05-09
Public Version Status
New
Public Device Record Key
dbfe0edc-8509-4dcc-a166-a9a233293633

Device Description

Gmax Pro Delivery System, Refurbished

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 00817495024592

Premarket Submissions

Submission Number Supplement Number
K140122 000