Sunshine Diamonds 836F314 010

by Dr. Hopf GmbH & Co. KG 2 variants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberESUN836F3140105 UDI-DI	Date23 Jun 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Sunshine Diamonds
Generic name: Diamond dental bur, reusable
Model / reference: 836F314 010

Primary DI / UDI-DI: ESUN836F3140105
FDA product code: DZP
GMDN term: Diamond dental bur, reusable

Device class: Class I
Regulation number: 872.4535
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Sunshine Diamonds A856 314 012

Class I
Sunshine Diamonds 850LC314 014

Class I

See all devices from Dr. Hopf GmbH & Co. KG →

Properties

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

Other properties (10)

Supplied sterile: No
Single 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