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Tubo Prescription Edgewise - Double Conv. .018" Ø.045" - Welding-16, 26, 36, 46…

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 20.40.330Model BRACKETS AND TUBES

by Dental Morelli Ltda.

Identity

Trade Name
Tubo Prescription Edgewise - Double Conv. .018" Ø.045" - Welding-16,26,36,46 - Central Hook EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic tube FDA UDI
Device Name
Tubo Prescription Edgewise - Double Conv. .018" Ø.045" - Welding-16,26,36,46 - Central Hook FDA UDI
Model / Reference
BRACKETS AND TUBES EUDAMED
20.40.330 EUDAMEDFDA UDI
Description
Tubo Prescription Edgewise - Double Conv. .018" Ø.045" - Welding-16,26,36,46 - Central Hook FDA UDI

Identifiers

Catalog Number
20.40.330 FDA UDI
Primary DI / UDI-DI
07895742180485 EUDAMEDFDA UDI
Basic UDI-DI
7895742122FU EUDAMED
B-07895742180485 EUDAMED
FDA Product Code
DZD FDA UDI
EMDN Code
Q010403 ORTHODONTIC BRACKETS AND BUTTONS EUDAMED
GMDN Term
Orthodontic tube 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

Tubo Prescription Edgewise - Double Conv. .018" Ø.045" - Welding-16, 26, 36, 46… by Dental Morelli Ltda. — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED…

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 d1f4df71-0877-4dd6-8323-634f9a75aaa3 61 fields · synced Jun 19, 2026
  • EUDAMED 84112d2e-df3e-4724-8bc9-14cc31f2e78b 61 fields · synced May 19, 2026
  • FDA UDI 05f6b6d2-2e23-4f5f-aa4d-29b5afaf9b88 35 fields · synced May 30, 2026