Identity
- Trade Name
- Straumann PrefGel FDA UDI
- Generic Name
- Dental root surface conditioner FDA UDI
- Device Name
- Straumann® PrefGel®, 5 x 0.6 ml (24% EDTA) FDA UDI
- Model / Reference
- PrefGel FDA UDI
- Description
- Straumann® PrefGel®, 5 x 0.6 ml (24% EDTA) FDA UDI
Identifiers
- Catalog Number
- 075.203W FDA UDI
- Primary DI / UDI-DI
- 07630031730053 FDA UDI
- 510(k) Number
- K063812 FDA UDI
- FDA Product Code
- KJJ FDA UDI
- GMDN Term
- Dental root surface conditioner FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 0.6 Milliliter FDA UDI
Category: Dental root surface conditioner
Straumann PrefGel by Institut Straumann SA — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Institut Straumann SA
Sources (1)
- FDA UDI 22a296bf-e892-4246-96ef-8daa4178d9a0 38 fields · synced May 30, 2026