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EndoPilot DownPack expansion set

FDA UDI

Class I (US FDA UDI)

by Schlumbohm GmbH & Co. KG

Identity

Trade Name
EndoPilot DownPack expansion set FDA UDI
Generic Name
Endodontic obturation system FDA UDI
Device Name
EndoPilot DownPack expansion set consist of: D-Pack handpiece, with LED-indicator, Heating-tip size: fine and a D-Pack/Backfill holder left FDA UDI
Model / Reference
v00 FDA UDI
Description
EndoPilot DownPack expansion set consist of: D-Pack handpiece, with LED-indicator, Heating-tip size: fine and a D-Pack/Backfill holder left FDA UDI

Identifiers

Catalog Number
110 0132-US FDA UDI
Primary DI / UDI-DI
04260482991135 FDA UDI
510(k) Number
K202906 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic obturation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endodontic obturation system

EndoPilot DownPack expansion set by Schlumbohm GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f794a81-e9bb-4bbb-80e3-73451fe59ffc 35 fields · synced May 30, 2026