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Elite®

FDA UDI

Class I (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name
Elite® FDA UDI
Generic Name
Orthodontic tube FDA UDI
Device Name
.018 UR6 CV STD -10T 0A 10O FDA UDI
Model / Reference
900-007-10 FDA UDI
Description
.018 UR6 CV STD -10T 0A 10O FDA UDI

Identifiers

Primary DI / UDI-DI
00190707050085 FDA UDI
FDA Product Code
DZD FDA UDI
GMDN Term
Orthodontic tube 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic tube

Elite® by Ortho Organizers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 10365f46-a049-4999-9b0d-578855131075 33 fields · synced Jun 9, 2026