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Intraoral Elastic - Latex - Medium 3/4"

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 60.01.340Model LATEX ELASTICSModel LATEX EXTRAORAL ELASTICS

by Dental Morelli Ltda.

Identity

Trade Name
Intraoral Elastic - Latex - Medium 3/4" EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic archwire/bracket ligature FDA UDI
Device Name
Intraoral Elastic - Latex - Medium 3/4" FDA UDI
Model / Reference
LATEX ELASTICS EUDAMED
60.01.340 EUDAMEDFDA UDI
LATEX EXTRAORAL ELASTICS EUDAMED
Description
Intraoral Elastic - Latex - Medium 3/4" FDA UDI

Identifiers

Catalog Number
60.01.340 FDA UDI
Primary DI / UDI-DI
07895742136789 EUDAMEDFDA UDI
Basic UDI-DI
7895742178GP EUDAMED
B-07895742136789 EUDAMED
FDA Product Code
ECI FDA UDI
EMDN Code
Q010404 ORTHODONTIC ELASTICS, CHAINS AND SPRINGS EUDAMED
GMDN Term
Orthodontic archwire/bracket ligature FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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

Yes

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

Category: Orthodontic retainer

Intraoral Elastic - Latex - Medium 3/4" by Dental Morelli Ltda. — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (3)

  • EUDAMED 219c0148-85e2-40df-8a40-f7b0ecd000de 61 fields · synced Jun 19, 2026
  • EUDAMED 451f0f73-2ece-4195-aeba-e616e4cbb321 61 fields · synced May 17, 2026
  • FDA UDI 97221eef-36fe-4e2e-b93d-6cf6ae72912b 35 fields · synced May 30, 2026