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Tip ClearLift QS CVD (Female)

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
Tip ClearLift QS CVD (Female) FDA UDI
Generic Name
Multi-modality skin surface treatment system FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Catalog Number
AACL02062120 FDA UDI
Primary DI / UDI-DI
17290110122246 FDA UDI
510(k) Number
K072564 FDA UDI
FDA Product Code
FTC FDA UDI
GEX FDA UDI
HHR FDA UDI
LNK FDA UDI
GMDN Term
Multi-modality skin surface treatment system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4630 FDA UDI
878.4810 FDA UDI
884.4550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality skin surface treatment system

Tip ClearLift QS CVD (Female) by Alma Lasers Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alma Lasers Ltd.

Sources (1)

  • FDA UDI f096b1ef-cff7-4680-bd0a-81e17f20cecd 34 fields · synced May 31, 2026