Hader 0101705

by PREAT Corporation

Hader 0101705 is a Class I device made by PREAT Corporation, listed in FDA GUDID since 24 Oct 2022 (UDI-DI 00842092105504), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00842092105504 UDI-DI	Date24 Oct 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00842092105504

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Hader
Generic name: Dental precision attachment fitting/adjustment tool
Model / Ref / Catalog: 0101705

Primary DI / UDI-DI: 00842092105504
FDA product code: NDP
GMDN term: Dental precision attachment fitting/adjustment tool

Device class: Class I
Regulation number: 872.3980
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Other devices filed under Dental precision attachment fitting/adjustment tool.

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Properties

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

Other properties (9, all answered No)