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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
Root canal post, preformed FDA UDI
Device Name
Root canal posts Mooser Adhesive head Ceramicor® Size 3 FDA UDI
Model / Reference
051034 FDA UDI
Description
Root canal posts Mooser Adhesive head Ceramicor® Size 3 FDA UDI

Identifiers

Catalog Number
051034 FDA UDI
Primary DI / UDI-DI
07640173090021 FDA UDI
FDA Product Code
ELR FDA UDI
GMDN Term
Root canal post, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3810 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 15.5 Millimeter FDA UDI

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

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 5dabd5a3-04ad-437b-8512-e19fce7348a3 37 fields · synced Jun 8, 2026