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Dentaprint

FDA UDI

Class I (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
Dentaprint FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Dentaprint 3D Ortho Model Resin Sample FDA UDI
Model / Reference
S3DOR FDA UDI
Description
Dentaprint 3D Ortho Model Resin Sample FDA UDI

Identifiers

Catalog Number
S3DOR FDA UDI
Primary DI / UDI-DI
E235S3DOR0 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, resin

Dentaprint by Shofu Dental Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

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 fcf366dc-0143-4330-94dc-6ec78382b0b3 35 fields · synced May 31, 2026