← 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 AMCOP BIOACTIVATOR HARD Class III Mod. TC Size 3 - 55 mm FDA UDI
Model / Reference
BIO-TC3HM FDA UDI
Description
Amcop Bioactivator AMCOP BIOACTIVATOR HARD Class III Mod. TC Size 3 - 55 mm FDA UDI

Identifiers

Catalog Number
BIO-TC3HM FDA UDI
Primary DI / UDI-DI
EMICBIOTC3HM1 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 ba76a6c0-6f37-4dc3-bc97-626f1f8c52f3 34 fields · synced May 31, 2026