Identity
- Trade Name
- Aurofluid 2 PF FDA UDI
- Generic Name
- Dental casting noble alloy FDA UDI
- Device Name
- Aurofluid 2 PF FDA UDI
- Model / Reference
- 01050010_1OZ FDA UDI
- Description
- Aurofluid 2 PF FDA UDI
Identifiers
- Catalog Number
- 01050010 FDA UDI
- Primary DI / UDI-DI
- 97640173080100 FDA UDI
- FDA Product Code
- EJT FDA UDI
- GMDN Term
- Dental casting noble alloy FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3060 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
High-level Disinfectant FDA UDI
Aurofluid 2 PF by Cendres+Métaux SA — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Cendres+Métaux SA
Sources (1)
- FDA UDI 937d00f4-8cee-4e28-8212-51ade4f711a6 36 fields · synced Jun 1, 2026