← Back to catalogue

AcuTip 500

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 7000278

by Cutera, Inc.

Identity

Trade Name
AcuTip 500 EUDAMEDFDA UDI
Generic Name
Light-energy skin surface treatment system applicator FDA UDI
Device Name
AcuTip 500 EUDAMED
AcuTip 500 IPL Handpiece FDA UDI
Model / Reference
7000278 EUDAMED
AcuTip 500 FDA UDI
Description
AcuTip 500 IPL Handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
00816722022103 EUDAMEDFDA UDI
Basic UDI-DI
B-00816722022103 EUDAMED
510(k) Number
K050047 FDA UDI
FDA Product Code
GEX FDA UDI
EMDN Code
Z12011019 MULTI–PLATFORM LASER EUDAMED
GMDN Term
Light-energy skin surface treatment system applicator FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

AcuTip 500 by Cutera, Inc. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cutera, Inc.
EUDAMED SRN
US-MF-000010456
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED cf71ebfd-2f90-4c39-8b31-e3706d8bd06f 61 fields · synced Jul 20, 2026
  • FDA UDI e99735e7-3779-466e-b4db-b7484c569c89 35 fields · synced May 30, 2026