FDA UDI In Commercial Distribution 🇺🇸 United States

ERISE Laser Handpiece

DI: 08034108512426 · Model: E262B1 · DEKA M.E.L.A. SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ERISE Laser Handpiece
Primary DI
08034108512426
Version / Model
E262B1
Company Name
DEKA M.E.L.A. SRL
Labeler DUNS
629381096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-16
Public Version
2
Public Version Date
2025-07-14
Public Version Status
Update
Public Device Record Key
8850500f-b8a6-4915-bf54-e2b59c8c736c

Device Description

ERISE Laser Handpiece is an Erbium:YAG laser handpiece delivering laser radiation at 2940nm. It is intended to be used with DEKA LUXEA platform, cleared by FDA with K192539. The ERISE Laser Handpiece includes: - a connector to connect to the console - a cord where electrical cables and hydraulic tubes pass in - a plastic shell - a laser cavity - a mechanical shutter - an optical guide - an ending tip which provides different spot sizes (diameter 2, 4, 9mm), including microbeam output (diameter 9mm). The 2940nm Erbium:YAG laser handpiece is controlled by the DEKA LUXEA console which it is connected to, through the connector.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47883 Dermatological solid-state laser system

Identifiers

Type ID
Primary 08034108512426

Premarket Submissions

Submission Number Supplement Number
K202258 000