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Spring paste fillers 25mm 040

FDA UDI

Class I (US FDA UDI)

by Diaswiss SA

Identity

Trade Name
Spring paste fillers 25mm 040 FDA UDI
Generic Name
Endodontic obturation material distribution endpiece, reusable FDA UDI
Device Name
Rotary instrument for endodontic intraoral use FDA UDI
Model / Reference
825025.040-0 FDA UDI
Description
Rotary instrument for endodontic intraoral use FDA UDI

Identifiers

Primary DI / UDI-DI
07630049954625 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Endodontic obturation material distribution endpiece, reusable 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

No

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: Endodontic obturation material distribution endpiece, reusable

Spring paste fillers 25mm 040 by Diaswiss SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation material distribution endpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diaswiss SA

Sources (1)

  • FDA UDI 6c824072-d48e-4f67-8694-32264b8dc4be 33 fields · synced Jun 8, 2026