FDA UDI In Commercial Distribution 🇺🇸 United States

FemiLift Sleeve

DI: 17290110121980 · Model: 1 · ALMA LASERS LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FemiLift Sleeve
Primary DI
17290110121980
Version / Model
1
Catalog Number
AACO28111924
Company Name
ALMA LASERS LTD.
Labeler DUNS
532283264
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-03
Public Version
2
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
1c453507-084e-4bf6-90ff-4198a609f0cf

Device Description

Package of 24 units

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
HQF Laser, Ophthalmic
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 17290110121980

Premarket Submissions

Submission Number Supplement Number
K103501 000