Prechopper 37-0024

by Charmant Inc.

Prechopper 37-0024 is a Class I device made by Charmant Inc., listed in FDA GUDID since 18 Sep 2023 (UDI-DI 00883475708417), 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	Number00883475708417 UDI-DI	Date18 Sep 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00883475708417

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Prechopper
Generic name: Ophthalmic surgical probe, reusable
Model / reference: 37-0024

Primary DI / UDI-DI: 00883475708417
FDA product code: HNQ
GMDN term: Ophthalmic surgical probe, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

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Other devices filed under Ophthalmic surgical probe, reusable.

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Properties

Sterilise before use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)