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Spring paste fillers 25mm 030, pu: 4 p

FDA UDI

Class I (US FDA UDI)

by Diaswiss SA

Identity

Trade Name
Spring paste fillers 25mm 030, pu: 4 p FDA UDI
Generic Name
Endodontic obturation material distribution endpiece, reusable FDA UDI
Device Name
Rotary instrument for endodontic intraoral use FDA UDI
Model / Reference
825025.030 FDA UDI
Description
Rotary instrument for endodontic intraoral use FDA UDI

Identifiers

Primary DI / UDI-DI
07630049992368 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 030, pu: 4 p 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 c0d3cbfa-55c7-438b-889a-6028a2d94df4 33 fields · synced Jun 8, 2026