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Composite Paste (Germany)

FDA UDI

Class I (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
Composite Paste (Germany) FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
Contains DI: E2350551GER0 FDA UDI
Model / Reference
001 FDA UDI
Description
Contains DI: E2350551GER0 FDA UDI

Identifiers

Catalog Number
0551-GER FDA UDI
Primary DI / UDI-DI
E2350551GER0 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dentifrice

Composite Paste (Germany) by Shofu Dental Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

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 9db06f53-701f-4d75-87c8-9c78a4a4a752 36 fields · synced Jun 1, 2026