Identity
- Trade Name
- Walser® Injecto-Löffel FDA UDI
- Generic Name
- Dental impression material kit, single-use FDA UDI
- Model / Reference
- 0 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04262363910761 FDA UDI
- FDA Product Code
- EHY FDA UDI
- GMDN Term
- Dental impression material kit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6880 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Walser® Injecto-Löffel by Dr. Walser Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 3e83c469-4752-4f4d-b7f4-ef1cfb0b97f2 33 fields · synced May 30, 2026