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MR Phaco PH6004

by Crestpoint Management Ltd.

MR Phaco PH6004 is a Class I device made by Crestpoint Management Ltd., listed in FDA GUDID since 2 Jun 2025 (UDI-DI G412PH60040), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG412PH60040 UDI-DI Date2 Jun 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • 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  • Withdrawn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
PH6004
Primary DI / UDI-DI
G412PH60040
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

Related devices

Category: Soft-tissue surgical hook, reusable

Similar devices in this category

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

Other devices from Crestpoint Management Ltd.

See all devices from Crestpoint Management Ltd. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)