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Aditek

FDA UDI

Class I (US FDA UDI)

by Aditek Do Brasil S/A

Identity

Trade Name
ADITEK FDA UDI
Generic Name
Orthodontic metal band FDA UDI
Device Name
Molar Band LL 28,5 w/10 FDA UDI
Model / Reference
04.01.3285 FDA UDI
Description
Molar Band LL 28,5 w/10 FDA UDI

Identifiers

Primary DI / UDI-DI
07899439202009 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic metal band FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Category: Orthodontic metal band

A comprehensive overview of the ADITEK molar band, including its features, benefits, and usage in orthodontic treatment.

Similar devices

Also classified as Orthodontic metal band.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fe6b79e-976c-4428-966a-2f3e614478e5 33 fields · synced Aug 3, 2026