Identity
- Trade Name
- Walser® matrix forceps FDA UDI
- Generic Name
- Rubber dam clamp forceps FDA UDI
- Device Name
- Walser® matrix forceps according to G. R. Daiger FDA UDI
- Model / Reference
- 036 FDA UDI
- Description
- Walser® matrix forceps according to G. R. Daiger FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04262363910006 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rubber dam clamp forceps
Walser® matrix forceps 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.
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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 a1eb0620-1670-4b24-92d1-90ea6f275182 33 fields · synced Jun 1, 2026