← Back to catalogue

Amcop Bioactivator

FDA UDI

Class I (US FDA UDI)

by Micerium Spa

Identity

Trade Name
Amcop Bioactivator FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
Amcop Bioactivator BIOACTIVATOR 1 pc. Class II Mod. SC DCM Size 2 - 50 mm FDA UDI
Model / Reference
BSC2-DCM FDA UDI
Description
Amcop Bioactivator BIOACTIVATOR 1 pc. Class II Mod. SC DCM Size 2 - 50 mm FDA UDI

Identifiers

Catalog Number
BSC2-DCM FDA UDI
Primary DI / UDI-DI
EMICBSC2DCM1 FDA UDI
FDA Product Code
KMY FDA UDI
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5525 FDA UDI
Commercial Distribution
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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic retainer

Amcop Bioactivator by Micerium Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Micerium Spa

Sources (1)

  • FDA UDI 56981e91-d7da-445d-885a-3ff91a987e81 34 fields · synced Jun 8, 2026