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Robot Point

FDA UDI

Class I (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
ROBOT POINT FDA UDI
Generic Name
Diamond dental bur, reusable FDA UDI
Device Name
ROBOT POINT SF301CR FDA UDI
Model / Reference
789V-1 FDA UDI
Description
ROBOT POINT SF301CR FDA UDI

Identifiers

Catalog Number
789V-1 FDA UDI
Primary DI / UDI-DI
E235789V10 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Diamond dental bur, reusable

A comprehensive medical device directory listing, providing detailed information on the ROBOT POINT, including its features, compliance, and usage.

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

Manufacturer
Shofu Dental Corp.

Sources (1)

  • FDA UDI 732130e1-1205-473e-b931-cf4914bd3a40 35 fields · synced Jul 26, 2026