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Walser® matrices

FDA UDI

Class I (US FDA UDI)

by Dr. Walser Dental GmbH

Identity

Trade Name
Walser® matrices FDA UDI
Generic Name
Rubber dam clamp forceps FDA UDI
Device Name
Set of 25 Walser® matrices with Walser® matrix forceps according to G. R. Daiger FDA UDI
Model / Reference
031 FDA UDI
Description
Set of 25 Walser® matrices with Walser® matrix forceps according to G. R. Daiger FDA UDI

Identifiers

Primary DI / UDI-DI
04262363910709 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Rubber dam clamp forceps 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusableDental matrix band, reusableRubber dam clamp forceps

Walser® matrices by Dr. Walser Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam clamp forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01759ed8-7c92-4eed-a246-e8b41d747ddb 33 fields · synced May 30, 2026