← Back to catalogue

Endodontic Posts

FDA UDI

Class I (US FDA UDI)

by Rhein 83 Srl

Identity

Trade Name
ENDODONTIC POSTS FDA UDI
Generic Name
Root canal post, preformed FDA UDI
Device Name
DISPOSABLE titanium device to be cemented into the root canal FDA UDI
Model / Reference
TITANIUM PIVOT KIT MICRO size mm.10 pz.5 FDA UDI
Description
DISPOSABLE titanium device to be cemented into the root canal FDA UDI

Identifiers

Catalog Number
036PTM10 FDA UDI
Primary DI / UDI-DI
08059224001159 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
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

Category: Root canal post, preformed

Endodontic Posts by Rhein 83 Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal post, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Rhein 83 Srl

Sources (1)

  • FDA UDI 543e840d-4c4f-40df-a187-cf2f757aeed7 34 fields · synced May 31, 2026