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Polodent Astringent Solution
EUDAMEDClass I (EU MDR)
Ref ALST20POLOModel Astringent solution
by Alan & Co
Identity
- Trade Name
- Polodent Astringent Solution EUDAMED
- Device Name
- Alstringent EUDAMED
- Model / Reference
- Astringent solution EUDAMEDALST20POLO EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05425032540631 EUDAMED
- Basic UDI-DI
- 542503254ALST7X EUDAMED
- EMDN Code
- Q019007 BUCCAL TOPICAL TREATMENT PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Polodent Astringent Solution by Alan & Co — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 542503254ALST7X | Class I | Active |
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Manufacturer
- Manufacturer
- Alan & Co
- EUDAMED SRN
- BE-MF-000000141
Sources (1)
- EUDAMED 627790eb-e11a-4a45-a628-e58b745456ef 61 fields · synced Jul 16, 2026