FDA UDI In Commercial Distribution 🇺🇸 United States

FemiLift Handpiece

DI: 17290110120785 · Model: 1 · ALMA LASERS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FemiLift Handpiece
Primary DI
17290110120785
Version / Model
1
Catalog Number
AACO17111361
Company Name
ALMA LASERS LTD.
Labeler DUNS
532283264
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
36269536-ecf8-42ab-8a11-7b27e8a233c6

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HQF Laser, Ophthalmic

GMDN Terms

Code Name
40781 Ultrasonic hyperthermia system

Identifiers

Type ID
Primary 17290110120785

Premarket Submissions

Submission Number Supplement Number
K103501 000