FDA UDI Not in Commercial Distribution 🇺🇸 United States

M22™

DI: 07290109140360 · Model: M22 · LUMENIS LTD.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
M22™
Primary DI
07290109140360
Version / Model
M22
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-14
Public Version
5
Public Version Date
2024-01-17
Public Version Status
Update
Public Device Record Key
c2318467-c2f3-4311-8597-1e0243b019be
Distribution End Date
2024-01-15

Device Description

M22, 1X IPL

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
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
ONG Powered Laser Surgical Instrument With Microbeam\Fractional Output

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 07290109140360

Customer Contacts

Phone
408-764-3000