FDA UDI In Commercial Distribution 🇺🇸 United States

PRISMA

DI: 08034108512464 · Model: M135A1 · DEKA M.E.L.A. SRL
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PRISMA
Primary DI
08034108512464
Version / Model
M135A1
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
2024-09-17
Public Version
2
Public Version Date
2025-03-04
Public Version Status
Update
Public Device Record Key
3412f2d4-2a4b-4fcd-91af-54f5245a362e

Device Description

The DEKA PRISMA is a device provided with two pulsed light handpieces and a RF handpiece. The overall weight is approximately 62 kg and the sizes 47 x 56 x 106 cm (LxWxH) without external parts and reclined display and 47 x 56 x 202 cm (LxWxH) with handpiece holders at maximum extension Electrical requirements: 115V~, 50/60Hz, 2300VA. The operator interacts directly with the external portions of the system displayed in the following.

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
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 08034108512464

Premarket Submissions

Submission Number Supplement Number
K233473 000
K250281 000