Identity
- Trade Name
- CEKA & PRECI-LINE ATTACHMENTS FDA UDI
- Generic Name
- Bar dental precision attachment FDA UDI
- Device Name
- REVAX M2 AXIAL FEMALE TI 1 P. FDA UDI
- Model / Reference
- RA 0091 FDA UDI
- Description
- REVAX M2 AXIAL FEMALE TI 1 P. FDA UDI
Identifiers
- Catalog Number
- RA 0091 FDA UDI
- Primary DI / UDI-DI
- 04260576942067 FDA UDI
- FDA Product Code
- EGG FDA UDI
- GMDN Term
- Bar dental precision attachment FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3165 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 2 Millimeter FDA UDI
Category: Bar dental precision attachment
Ceka & Preci-Line Attachments by Alpha-Dent — 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
- Alpha-Dent
Sources (1)
- FDA UDI 32cbdfb2-444a-4122-ab2f-53d6cb66d6fc 36 fields · synced Jun 1, 2026