FDA UDI In Commercial Distribution 🇺🇸 United States

Matrix Pro Applicator, Profound Matrix

DI: 00817495023731 · Model: FG71851 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Matrix Pro Applicator, Profound Matrix
Primary DI
00817495023731
Version / Model
FG71851
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-16
Public Version
3
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
3e9369cf-927f-4262-91db-57de4a54487d

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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 00817495023731
Previous 07290109952956

Premarket Submissions

Submission Number Supplement Number
K211217 000