Amcop Bioactivator BS5-DTM
by Micerium SpA
Ref BS5-DTMModel Micerium AMCOP Bioactivators
Amcop Bioactivator BS5-DTM is a Class I device made by Micerium SpA, registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI ++EMICFAM8BVW) and listed in FDA GUDID since 5 Aug 2024 (UDI-DI EMICBS5DTM1), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number++EMICFAM8BVW EMICBS5DTM1 | Date12 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberEMICBS5DTM1 | Date5 Aug 2024 | StatusListed |
Official records
- EUDAMED public site ++EMICFAM8BVW
Across registries
- EUDAMED Basic UDI-DI ++EMICFAM8BVW registered 12 Jun 2026 Active
- FDA GUDID UDI-DI EMICBS5DTM1 listed 5 Aug 2024 Listed
Timeline
- Listed FDA GUDID EMICBS5DTM1
- Registered EUDAMED ++EMICFAM8BVW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Amcop Bioactivator
- Generic name
- Orthodontic retainer
- Device name
- Micerium AMCOP Bioactivators / Micerium AMCOP Bioactivators
- Model / Ref / Catalog
- BS5-DTM, Micerium AMCOP Bioactivators
- Primary DI / UDI-DI
- EMICBS5DTM1
- Basic UDI-DI
- ++EMICFAM8BVW
- FDA product code
- KMY
- EMDN code
- Q010499 Orthodontic devices - other
- GMDN term
- Orthodontic retainer
- Device class
- Class I
- Regulation number
- 872.5525
- EU registration type
- Standard device
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
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