Identity
- Trade Name
- R.T.R. Syringe FDA UDI
- Generic Name
- Synthetic bone graft FDA UDI
- Device Name
- Single-use, sterile resorbable bone substitute FDA UDI
- Model / Reference
- 01S0500 FDA UDI
- Description
- Single-use, sterile resorbable bone substitute FDA UDI
Identifiers
- Catalog Number
- 01S0500 FDA UDI
- Primary DI / UDI-DI
- 03760140702987 FDA UDI
- FDA Product Code
- LYC FDA UDI
- GMDN Term
- Synthetic bone graft FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3930 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 0.8 Milliliter FDA UDI
Category: Synthetic bone graft
R.T.R. Syringe by Septodont Sas Specialites Septodont — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Septodont Sas Specialites Septodont
Sources (1)
- FDA UDI 3c3c0d01-dc2b-4a37-9250-66af3568986b 36 fields · synced May 30, 2026