← Back to catalogue

Alice

FDA UDI

Class II (US FDA UDI)

by Rmo

Identity

Trade Name
Alice FDA UDI
Generic Name
Orthodontic bracket, plastic, single-use FDA UDI
Device Name
STD EDG ALICE 1-2 BIC MX/MN 018R/L FDA UDI
Model / Reference
C02006 FDA UDI
Description
STD EDG ALICE 1-2 BIC MX/MN 018R/L FDA UDI

Identifiers

Primary DI / UDI-DI
00885797489401 FDA UDI
FDA Product Code
DYW FDA UDI
GMDN Term
Orthodontic bracket, plastic, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

Yes

FDA UDI

Category: Orthodontic bracket, plastic, single-use

Alice by Rmo — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, plastic, single-use.

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

Manufacturer
Rmo

Sources (1)

  • FDA UDI 34a0f458-d6ff-40c8-a42d-4cb9c66eb8d5 33 fields · synced Jun 1, 2026