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Root canal posts Mooser

FDA UDI

Class I (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
Root canal posts Mooser FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
Root canal posts Mooser Pilot reamer (White) Post size 1 FDA UDI
Model / Reference
072314 FDA UDI
Description
Root canal posts Mooser Pilot reamer (White) Post size 1 FDA UDI

Identifiers

Catalog Number
072314 FDA UDI
Primary DI / UDI-DI
07640166512608 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rotary/reciprocating endodontic file/rasp, reusable

Root canal posts Mooser by Cendres+Métaux SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cendres+Métaux SA

Sources (1)

  • FDA UDI 68f734db-3381-47f8-bee0-5461ede9a245 35 fields · synced May 30, 2026