← Back to catalogue

Beta-T

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
BETA-T FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
.016 X .022 BETA-T MUSHROOM LOOP RIGHT FORM 38MM (5) FDA UDI
Model / Reference
.016 X .022 MUSHROOM LOOP ARCHWIRE 38MM FDA UDI
Description
.016 X .022 BETA-T MUSHROOM LOOP RIGHT FORM 38MM (5) FDA UDI

Identifiers

Catalog Number
228-638M FDA UDI
Primary DI / UDI-DI
D909228638 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic archwire 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire

Beta-T by Ortho Arch Company Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic archwire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a661ae0a-9863-45c5-a3ce-b45feb275875 34 fields · synced May 30, 2026