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Centrix Endo Kit

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Centrix Endo Kit FDA UDI
Generic Name
Calcium hydroxide dental suspension FDA UDI
Device Name
Centrix Endo Kit root canal pack FDA UDI
Model / Reference
360053 FDA UDI
Description
Centrix Endo Kit root canal pack FDA UDI

Identifiers

Primary DI / UDI-DI
00817051021218 FDA UDI
FDA Product Code
EMA FDA UDI
EJK FDA UDI
GMDN Term
Calcium hydroxide dental suspension FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
872.3250 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Calcium hydroxide dental suspension

Centrix Endo Kit by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Calcium hydroxide dental suspension.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI b82eadb3-9aa3-496b-9e36-15787285ef43 33 fields · synced Jun 8, 2026