FDA UDI In Commercial Distribution 🇺🇸 United States

Standard 64 Sublative iD, (100 Pulse), 10-Pk

DI: 00817495024318 · Model: KT72861 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Standard 64 Sublative iD, (100 Pulse), 10-Pk
Primary DI
00817495024318
Version / Model
KT72861
Catalog Number
KT72861
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
3336d55b-bb0d-437b-a1cb-3d7217b55b3d

Device Description

Standard 64 Sublative iD, (100 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
Yes
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 00817495024318

Premarket Submissions

Submission Number Supplement Number
K141507 000