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CytoPeel

FDA UDI

Class I (US FDA UDI)

by Emage Medical, Llc

Identity

Trade Name
CytoPeel FDA UDI
Generic Name
Multi-modality skin surface treatment system FDA UDI
Device Name
Powered Dermabrasion Device FDA UDI
Model / Reference
CP3 FDA UDI
Description
Powered Dermabrasion Device FDA UDI

Identifiers

Primary DI / UDI-DI
00860012651009 FDA UDI
FDA Product Code
GFE FDA UDI
GMDN Term
Multi-modality skin surface treatment system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality skin surface treatment system

CytoPeel by Emage Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Emage Medical, Llc

Sources (1)

  • FDA UDI b67183d6-4a52-459e-bb0e-da5fe3a95496 33 fields · synced May 30, 2026