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Elastic Ligature Applicator - Plastic

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 75.01.003Model REUSABLE INSTRUMENTS

by Dental Morelli Ltda.

Identity

Trade Name
Elastic Ligature Applicator - Plastic EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic elastomeric appliance pusher FDA UDI
Device Name
Elastic Ligature Applicator - Plastic FDA UDI
Model / Reference
REUSABLE INSTRUMENTS EUDAMED
75.01.003 EUDAMEDFDA UDI
Description
Elastic Ligature Applicator - Plastic FDA UDI

Identifiers

Catalog Number
75.01.003 FDA UDI
Primary DI / UDI-DI
07895742002688 EUDAMEDFDA UDI
Basic UDI-DI
B-07895742002688 EUDAMED
7895742133FZ EUDAMED
FDA Product Code
ECP FDA UDI
EMDN Code
L150701 ORTHODONTIC LIGATURE TOOLS, REUSABLE EUDAMED
GMDN Term
Orthodontic elastomeric appliance pusher FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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
Sterilization Method
Dry Heat Sterilization FDA UDI

Elastic Ligature Applicator - Plastic by Dental Morelli Ltda. — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 8cd8b5bb-9fdd-4f69-8de1-eb41c1062fee 61 fields · synced Jul 18, 2026
  • EUDAMED 3b6f116a-0f98-41b7-b96d-66a2effb9e54 61 fields · synced May 19, 2026
  • FDA UDI e5284774-7ce6-4b2d-a12c-d093b1866093 35 fields · synced May 30, 2026