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Bracket Prescription Roth - Light .022" - 22

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 10.10.403Model BRACKETS AND TUBES

by Dental Morelli Ltda.

Identity

Trade Name
Bracket Prescription Roth - Light .022" - 22 EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
Bracket Prescription Roth - Light .022" - 22 FDA UDI
Model / Reference
BRACKETS AND TUBES EUDAMED
10.10.403 EUDAMEDFDA UDI
Description
Bracket Prescription Roth - Light .022" - 22 FDA UDI

Identifiers

Catalog Number
10.10.403 FDA UDI
Primary DI / UDI-DI
07895742020057 EUDAMEDFDA UDI
Basic UDI-DI
B-07895742020057 EUDAMED
7895742122FU 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
Portugal 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

Yes

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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthodontic tube

Bracket Prescription Roth - Light .022" - 22 by Dental Morelli Ltda. — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Orthodontic tube.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
BR-MF-000004812
Authorised Representative
Nuno Flores PT-AR-000003118

Sources (3)

  • EUDAMED b0270224-369a-4a9f-bc1a-7903d03d8cd0 61 fields · synced Jul 14, 2026
  • EUDAMED b0270224-369a-4a9f-bc1a-7903d03d8cd0 61 fields · synced May 19, 2026
  • FDA UDI bf9790c0-e081-41c4-9747-ac78de281a05 35 fields · synced May 30, 2026