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Temphase

FDA UDI

Class I (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Temphase FDA UDI
Generic Name
Dental material mixing nozzle FDA UDI
Device Name
Mixing Tips; Refill FDA UDI
Model / Reference
28075 FDA UDI
Description
Mixing Tips; Refill FDA UDI

Identifiers

Catalog Number
28075 FDA UDI
Primary DI / UDI-DI
10841396101356 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental material mixing nozzle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

Category: Dental material mixing nozzle

Temphase by Kerr Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material mixing nozzle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 3ff396c1-293c-47c0-aa0d-724b4447ba18 35 fields · synced Jun 8, 2026