FDA UDI In Commercial Distribution 🇺🇸 United States

ClearLift Depth Control Set for ClearLift QS 5x5 (No Lasing Tip) Female

DI: 17290110122239 · Model: 1 · ALMA LASERS LTD.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ClearLift Depth Control Set for ClearLift QS 5x5 (No Lasing Tip) Female
Primary DI
17290110122239
Version / Model
1
Catalog Number
EGGG29112199
Company Name
ALMA LASERS LTD.
Labeler DUNS
532283264
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-30
Public Version
2
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
a60c1358-7698-45d8-b5bc-b8500bb59d7c

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
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
GEX Powered Laser Surgical Instrument
FTC Light, Ultraviolet, Dermatological
HHR Laser, Surgical, Gynecologic
LNK Laser For Gastro-Urology Use

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 17290110122239

Premarket Submissions

Submission Number Supplement Number
K072564 000