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Exceed

FDA UDI

Class II (US FDA UDI)

by MT.DERM GmbH

Identity

Trade Name
Exceed FDA UDI
Generic Name
Cosmetic micro-needling electronic handpiece, professional FDA UDI
Device Name
The Exceed microneedling device is intended to create many, very tiny, microscopic punctures in the epidermal and dermal layers of the skin using sterile stainless steel needles. Exceed consists of - Control Unit - Handpiece with handpiece cable - Handpiece Holder - Power Supply - Instructions for Use FDA UDI
Model / Reference
AD61USMP FDA UDI
Description
The Exceed microneedling device is intended to create many, very tiny, microscopic punctures in the epidermal and dermal layers of the skin using sterile stainless steel needles. Exceed consists of - Control Unit - Handpiece with handpiece cable - Handpiece Holder - Power Supply - Instructions for Use FDA UDI

Identifiers

Catalog Number
AD61USMP FDA UDI
Primary DI / UDI-DI
EMTDAD61USMP1 FDA UDI
FDA Product Code
QAI FDA UDI
GMDN Term
Cosmetic micro-needling electronic handpiece, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4430 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Exceed by MT.DERM GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MT.DERM GmbH

Sources (1)

  • FDA UDI 875fb118-fe95-4e7a-b3e5-61dc1defe9e3 36 fields · synced Jun 8, 2026