- Role
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DE-MF-000005784Exceed is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MT.DERM GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Apr 28, 2026
++EMTDMN1HMPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
+EMTDAD61MP0
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
2 warnings recorded — scroll inside the panel to see all entries.
The treatment of mucous membrane and eyeballs is strictly forbidden. The treatment must be immediately aborted in the event of excessive perception of pain and fainting/dizziness..
Do not perform microneedling in patients with haemophilia or other coagulation disorders; patients receiving anticoagulant or antiplatelet therapy (e.g. acetylsalicylic acid/aspirin, warfarin, heparin); uncontrolled diabetes mellitus; active acne in the treatment area; dermatoses in the treatment area (including skin tumours, keloids or predisposition to keloid formation, actinic/solar keratosis, warts, or suspicious moles); open wounds, eczema, or skin rashes in the treatment area; scars less than 6 months old; systemic or local active infections (including hepatitis A–F, HIV, herpes, rosacea, or other acute skin infections); during chemotherapy, radiotherapy, or high-dose corticosteroid therapy (from 4 weeks before until 4 weeks after treatment); within 12 months after plastic surgery in the treatment area; within 6 months after dermal filler injections in the treatment area; known allergy to topical/local anaesthetics; patients under the influence of alcohol or recreational drugs; and during pregnancy or lactation.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 29, 2018 | Dec 31, 2099 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
+EMTDAD61MP0Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++EMTDMN1HMAD61MPUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
1 packaging level registered — each level carries its own UDI-DI.
+EMTDAD61MP0× 1 unitBase unit+EMTDAD61MP1× 1 unitEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
Z12040203DERMAL REGENERATION EQUIPMENTNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
G10 067752 0020IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
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