FDA UDI In Commercial Distribution 🇺🇸 United States

Matrix Pro Cartridge box (pack of 7)

DI: 00817495023717 · Model: KT78161 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Matrix Pro Cartridge box (pack of 7)
Primary DI
00817495023717
Version / Model
KT78161
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
a28b4d3f-44a1-4907-a44a-49e692bf574f

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
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 00817495023717
Previous 47290109952961

Premarket Submissions

Submission Number Supplement Number
K211217 000