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Horico

FDA UDI

Class I (US FDA UDI)

by Hopf, Ringleb & Co. GmbH & Cie.

Identity

Trade Name
HORICO FDA UDI
Generic Name
Dental abrasive disk, reusable FDA UDI
Device Name
Diamond Disk FDA UDI
Model / Reference
W 352 190 FDA UDI
Description
Diamond Disk FDA UDI

Identifiers

Primary DI / UDI-DI
EHORW3521902 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental abrasive disk, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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: Dental abrasive disk, reusable

Horico by Hopf, Ringleb & Co. GmbH & Cie. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive disk, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hopf, Ringleb & Co. GmbH & Cie.

Sources (1)

  • FDA UDI 940c4a1f-0437-4624-a351-1f21cef58b3a 33 fields · synced Jun 1, 2026