← Back to catalogue

Dolder® System

FDA UDI

Class I (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
Dolder® System FDA UDI
Generic Name
Dental precision attachment fitting/adjustment tool FDA UDI
Device Name
Dolder® System Desactivator macro FDA UDI
Model / Reference
070201 FDA UDI
Description
Dolder® System Desactivator macro FDA UDI

Identifiers

Catalog Number
070201 FDA UDI
Primary DI / UDI-DI
07640166511847 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental precision attachment fitting/adjustment tool FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental precision attachment fitting/adjustment tool

Dolder® System by Cendres+Métaux SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental precision attachment fitting/adjustment tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cendres+Métaux SA

Sources (1)

  • FDA UDI 8a04f84f-eefe-480d-9f23-208cadc495ee 35 fields · synced Jun 1, 2026