← Back to catalogue

Traction device with safety breakaway - White - Medium force - 500gf

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 70.42.202Model AUXILIARY ORTHODONTIC COMPONENTS

by Dental Morelli Ltda.

Identity

Trade Name
Traction device with safety breakaway - White - Medium force - 500gf EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
Traction device with safety breakaway - White - Medium force - 500gf FDA UDI
Model / Reference
AUXILIARY ORTHODONTIC COMPONENTS EUDAMED
70.42.202 EUDAMEDFDA UDI
Description
Traction device with safety breakaway - White - Medium force - 500gf FDA UDI

Identifiers

Catalog Number
70.42.202 FDA UDI
Primary DI / UDI-DI
07895742002220 EUDAMEDFDA UDI
Basic UDI-DI
B-07895742002220 EUDAMED
7895742132FX EUDAMED
FDA Product Code
KCR FDA UDI
EMDN Code
Q010499 ORTHODONTIC DEVICES - OTHER EUDAMED
GMDN Term
Orthodontic extraoral headgear FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3220 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

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

Traction device with safety breakaway - White - Medium force - 500gf by Dental Morelli Ltda. — Class I — 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 4fa11f8c-d5f9-41a0-bd2e-c0650aaa2c61 61 fields · synced Jul 31, 2026
  • EUDAMED 200aaabc-5792-41e9-8af7-bc9a3a3f3ecf 61 fields · synced May 19, 2026
  • FDA UDI c05dd2d2-cc6d-48be-a852-4ed4fb68a125 35 fields · synced May 30, 2026