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
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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Dr. Walser Dental GmbH
Sources (1)
- FDA UDI 01759ed8-7c92-4eed-a246-e8b41d747ddb 33 fields · synced May 30, 2026