Rmo A01205

by Rmo

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00885797634795 UDI-DI	Date20 Aug 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Rmo
Generic name: Orthodontic archwire
Model / reference: A01205
Description: SHORT LIG TIE HK .014 PKG 100

Primary DI / UDI-DI: 00885797634795
FDA product code: DZC
GMDN term: Orthodontic archwire

Device class: Class I
Regulation number: 872.5410
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Prescription use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (10)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Serial number: No
Expiration date: No