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SeptoDiscs Mandrel Refill: 1 mandrel pop

FDA UDI

Class I (US FDA UDI)

by Septodont Sas Specialites Septodont

Identity

Trade Name
SeptoDiscs Mandrel Refill: 1 mandrel pop FDA UDI
Generic Name
Dental mandrel FDA UDI
Device Name
Mandrel for contra angle FDA UDI
Model / Reference
01C4030 FDA UDI
Description
Mandrel for contra angle FDA UDI

Identifiers

Catalog Number
01C4030 FDA UDI
Primary DI / UDI-DI
07897990328411 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental mandrel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental mandrel

SeptoDiscs Mandrel Refill: 1 mandrel pop by Septodont Sas Specialites Septodont — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mandrel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8dd551de-4827-44e9-9601-68293ff425da 34 fields · synced May 30, 2026