ADAMO S.r.l.
Italy IT-MF-000028175 Last updated 17 Sep 2026
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- Devices
- 30
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
LAMP015 Ref LAMP015
LAMP005 Ref LAMP005
ATON 2000 Plus Ref ATON-2000 Plus
KV40VL Ref KV40VL
ATON 1000 Lite Ref ATON-1000 Lite
LAMP017 Ref LAMP017
LAMP003 Ref LAMP003
LAMP020 Ref LAMP020
GELVDS50 Ref GELVDS50
Aton-2000 Ref ATON-2000
LIQPLZ100 Ref LIQPLZ100
LIQVCS30 Ref LIQVCS30
ISIDE β (Beta) Ref ISIDE β (Beta)
KV40 Ref KV40
ISIDE α (Alfa) Ref ISIDE α (Alfa)
KV30nb Ref KV30nb
ISIDE γ (Gamma) Ref ISIDE γ (Gamma)
Aton 1000 Ref ATON-1000
HS600 Ref HS600
Aton 100 Ref ATON-100
KV30 Ref KV30
HS650 Ref HS650
HORUS - HS series Ref HS200
KV20 Ref KV20
HS400 Ref HS400
HS450 Ref HS450
HS150 Ref HS150
HORUS - HS series Ref HS1000
HS800 Ref HS800
HORUS - HS series Ref HS100
About
Buy online dermatoscopes and professional accessories Adamo S.r.l. — ATON line, consumables and accessories Made in Italy for dermatologists and medical specialists.
What ADAMO S.r.l. makes
ADAMO S.r.l. manufactures endoscopic imaging systems, including the ISIDE series (β, α, γ), the ATON series, the HORUS HS series, and the KolpoView KV series (KV30nb, KV40). These devices are designed for internal medical examinations, such as cystoscopy and endoscopic procedures, providing visual diagnostics for clinical assessment.
The company’s products fall under EU Class I medical devices and are registered in the EUDAMED database. ADAMO S.r.l. is based in Italy and adheres to EU regulatory requirements for Class I devices.
Frequently asked questions
What types of medical devices does ADAMO S.r.l. manufacture?
ADAMO S.r.l. specializes in endoscopic imaging systems, including the ISIDE series (such as ISIDE β, ISIDE α, and ISIDE γ), the ATON series, the HORUS HS series, and the KolpoView KV series (e.g., KV30nb and KV40). These devices are primarily used for internal medical examinations like cystoscopy and other endoscopic procedures, enabling visual diagnostics for clinical assessment.
Where is ADAMO S.r.l. based, and what regulatory framework does it follow?
ADAMO S.r.l. is based in Italy. Its devices are classified under EU Class I, meaning they are considered low-risk medical devices. As such, they must comply with EU regulatory requirements, including registration in the EUDAMED database, which is the official EU database for medical devices.
Are ADAMO S.r.l.’s devices listed in any regulatory registries?
Yes, ADAMO S.r.l.’s devices are registered in the EUDAMED database. This registry is the central EU system for tracking medical devices, ensuring transparency and compliance with EU regulations for manufacturers and authorities.
How are ADAMO S.r.l.’s devices classified under EU regulations?
ADAMO S.r.l.’s devices fall under EU Class I classification. This classification is assigned based on risk assessment criteria outlined in EU medical device regulations. Class I devices are generally considered low-risk, often involving minimal intervention or direct patient contact without invasive procedures, but they still require compliance with EU regulatory standards.
Information
- Country
- Italy
- Address
- 1/B, Via Francesco Culcasi, TRAPANI, Italy
- Website
- www.adamosrl.com
- [email protected]
- Phone
- +39 0923 558778
- PRRC contact
- Alessio Adamo
- EUDAMED SRN
- IT-MF-000028175