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Sunshine Diamonds

FDA UDI

Class I (US FDA UDI)

by Dr. Hopf GmbH & Co. KG

Identity

Trade Name
Sunshine Diamonds FDA UDI
Generic Name
Diamond dental bur, reusable FDA UDI
Device Name
Rotary diamond instruments FDA UDI
Model / Reference
A801 314 033 FDA UDI
Description
Rotary diamond instruments FDA UDI

Identifiers

Primary DI / UDI-DI
ESUNA8013140332 FDA UDI
FDA Product Code
DZP FDA UDI
GMDN Term
Diamond dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4535 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Diamond dental bur, reusable

Sunshine Diamonds by Dr. Hopf GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diamond dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0c48c74-e873-4ff1-9e26-8d9871eb4d32 33 fields · synced May 31, 2026