MR Phaco PH1793RT

by Crestpoint Management Ltd.

MR Phaco PH1793RT is a Class I device made by Crestpoint Management Ltd., listed in FDA GUDID since 2 Jun 2025 (UDI-DI G412PH1793RT0), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberG412PH1793RT0 UDI-DI	Date2 Jun 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: MR Phaco
Generic name: Soft-tissue surgical hook, reusable
Model / reference: PH1793RT

Primary DI / UDI-DI: G412PH1793RT0
FDA product code: HNQ
GMDN term: Soft-tissue surgical hook, reusable

Device class: Class I
Regulation number: 886.4350
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Soft-tissue surgical hook, reusable.

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MR Phaco PH6004

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See all devices from Crestpoint Management Ltd. →

Properties

Sterilise before use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (11, all answered No)