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Mp-Post

FDA UDI

Class I (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
MP-POST FDA UDI
Generic Name
Steel dental bur, reusable FDA UDI
Device Name
MP-Post root canal drill black, size 5 FDA UDI
Model / Reference
MD.200004459 FDA UDI
Description
MP-Post root canal drill black, size 5 FDA UDI

Identifiers

Catalog Number
MD.200004459 FDA UDI
Primary DI / UDI-DI
07640166515364 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Steel dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Commercial Distribution
Not 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

Mp-Post 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 74a8bbac-d06a-4d4c-84f5-37848ffb9c1c 36 fields · synced Jun 6, 2026