FDA UDI Not in Commercial Distribution 🇺🇸 United States

Standard 64 Sublative iD, (200 Pulse), 10-Pk

DI: 37290109951196 · Model: KT72931 · SYNERON MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Standard 64 Sublative iD, (200 Pulse), 10-Pk
Primary DI
37290109951196
Version / Model
KT72931
Catalog Number
KT72931
Company Name
SYNERON MEDICAL LTD
Labeler DUNS
532685716
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
7
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
f5f6566f-21be-4b54-a5ff-a306df7b586e
Distribution End Date
2023-10-16

Device Description

Standard 64 Sublative iD, (200 Pulse), 10-Pk

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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 37290109951196

Premarket Submissions

Submission Number Supplement Number
K141507 000