← Back to catalogue

Bracket Biomax 022 Mbt Lr5 -17°t 0°a 4°o W/10

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 05.04.0885Model Orthodontic Brackets

by Aditek do Brasil SA

Identity

Trade Name
BRACKET BIOMAX 022 MBT LR5 -17°T 0°A 4°O W/10 EUDAMED
ADITEK FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
Bracket BioMax 022 MBT LR5 -17°T 0°A 4°O w/10 FDA UDI
Model / Reference
Orthodontic Brackets EUDAMED
05.04.0885 EUDAMEDFDA UDI
Description
Bracket BioMax 022 MBT LR5 -17°T 0°A 4°O w/10 FDA UDI

Identifiers

Primary DI / UDI-DI
07899439296237 EUDAMEDFDA UDI
Basic UDI-DI
7899439205J4 EUDAMED
FDA Product Code
EJF FDA UDI
EMDN Code
Q010403 ORTHODONTIC BRACKETS AND BUTTONS EUDAMED
GMDN Term
Orthodontic bracket, metal FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic tube

Bracket Biomax 022 Mbt Lr5 -17°t 0°a 4°o W/10 by Aditek do Brasil SA — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic tube.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Aditek do Brasil SA
EUDAMED SRN
BR-MF-000018793
Authorised Representative
EC Certification Service GmbH AT-AR-000006658

Sources (2)

  • EUDAMED dd4c09ec-2872-489c-94cc-c7ed303296a3 61 fields · synced Jul 29, 2026
  • FDA UDI 7372b34a-b4e3-42dc-873f-2b72fead5fed 33 fields · synced May 30, 2026