FDA UDI In Commercial Distribution 🇺🇸 United States

Dermal applicator

DI: 00817495023700 · Model: FG70523 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dermal applicator
Primary DI
00817495023700
Version / Model
FG70523
Catalog Number
FG70523
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-20
Public Version
1
Public Version Date
2023-10-30
Public Version Status
New
Public Device Record Key
6237b5ad-f836-4561-8b34-c2cded35b3c9

Device Description

Dermal applicator, Packaged, Profound

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 00817495023700
Previous 07290109952055

Premarket Submissions

Submission Number Supplement Number
K161043 000