FDA UDI In Commercial Distribution 🇺🇸 United States

Standard 64 Sublative iD (200 Pulse)

DI: 00817495023793 · Model: AS79333 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Standard 64 Sublative iD (200 Pulse)
Primary DI
00817495023793
Version / Model
AS79333
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-20
Public Version
5
Public Version Date
2023-07-17
Public Version Status
Update
Public Device Record Key
14d221d6-8286-416f-b62f-80c313b0aa80

Device Description

Standard 64 Sublative iD, (200 Pulse), Sterile

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 00817495023793
Previous 07290109951195

Premarket Submissions

Submission Number Supplement Number
K141507 000