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Endosolv E

FDA UDI

Class II (US FDA UDI)

by Septodont Sas Specialites Septodont

Identity

Trade Name
ENDOSOLV E FDA UDI
Generic Name
Root canal filling-removal solution FDA UDI
Device Name
Root canal filling solvant FDA UDI
Model / Reference
01E0260 FDA UDI
Description
Root canal filling solvant FDA UDI

Identifiers

Catalog Number
01E0260 FDA UDI
Primary DI / UDI-DI
03760140703298 FDA UDI
FDA Product Code
KIF FDA UDI
GMDN Term
Root canal filling-removal solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3820 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 13 Milliliter FDA UDI

Category: Root canal filling-removal solution

Endosolv E by Septodont Sas Specialites Septodont — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal filling-removal solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 64df8318-e02c-4439-afa2-76ab7339a21c 36 fields · synced May 30, 2026