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Bracket Roth Prescription - Ceramic SLP .022" - 22

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 10.16.004Model BRACKETS AND TUBES

by Dental Morelli Ltda.

Identity

Trade Name
Bracket Roth Prescription - Ceramic SLP .022" - 22 EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
Bracket Roth Prescription - Ceramic SLP .022" - 22 FDA UDI
Model / Reference
BRACKETS AND TUBES EUDAMED
10.16.004 EUDAMEDFDA UDI
Description
Bracket Roth Prescription - Ceramic SLP .022" - 22 FDA UDI

Identifiers

Catalog Number
10.16.004 FDA UDI
Primary DI / UDI-DI
07895742282134 EUDAMEDFDA UDI
Basic UDI-DI
B-07895742282134 EUDAMED
7895742122FU EUDAMED
FDA Product Code
NJM FDA UDI
EMDN Code
Q010403 ORTHODONTIC BRACKETS AND BUTTONS EUDAMED
GMDN Term
Orthodontic bracket, ceramic FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.5470 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

No

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

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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 07bfc810-c6b8-4745-a8ed-dec0359754f8 61 fields · synced Jul 29, 2026
  • EUDAMED 05d89358-2909-4926-8df6-65e29e20d1b8 61 fields · synced May 19, 2026
  • FDA UDI 0ff8b4c0-d004-4439-846f-51b0dda40694 35 fields · synced May 30, 2026