FDA UDI Not in Commercial Distribution 🇺🇸 United States

Dermal Single- Use Cartridge 6-Pkg, Profound,

DI: 27290109950826 · Model: KT76653 · SYNERON MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dermal Single- Use Cartridge 6-Pkg, Profound,
Primary DI
27290109950826
Version / Model
KT76653
Catalog Number
KT76653
Company Name
SYNERON MEDICAL LTD
Labeler DUNS
532685716
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
4
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
ada72747-276c-439c-a581-317332c4e505
Distribution End Date
2023-10-16

Device Description

Dermal Single- Use Cartridge 6-Pkg, Profound,

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 27290109950826