FRIOS®
- Primary DI
- 07392532232909
- Brand
- FRIOS®
- Company
- Dentsply Implants Manufacturing GmbH
- Model
- 51-4093
- Catalog number
- 51-4093
- Device description
- Bone Stud Remover
- Published
- 2022-07-14
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Product Codes
| Code | Name |
|---|---|
| NDP | Accessories, implant, dental, endosseous |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| NDP | Accessories, Implant, Dental, Endosseous | Dental | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07392532232909 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07392532232909 | 07392532232909 | 7392532232909 |
GMDN Terms
| Term | Definition |
|---|---|
| Dental elevator, tooth/root | A hand-held, manual, dental surgical instrument intended to be used as a lever during the extraction of a tooth or retained roots. It is typically a one-piece instrument with a strong but slender blade at the distal working end, or it may be double-ended with a central handle. It is available in a variety of sizes and blade designs and is pushed in between the gums and the tooth exterior to loosen the tissue surrounding the tooth. Sometimes this can be enough to loosen and extract the tooth without the use of other instruments. This is a reusable device. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 344038836
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 07392532236020 | SIMPLANT® | 54500214 | 54500214 | 2026-03-10 |
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| 07392532281280 | ATLANTIS® | 68020076 | 68020076 | 2025-12-18 |
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| 07392532215339 | ANKYLOS® | 31021160 | 31021160 | 2020-11-18 |
| 07392532215353 | ANKYLOS® | 31021180 | 31021180 | 2020-11-18 |
| 07392532215865 | ANKYLOS® | 31021630 | 31021630 | 2020-11-18 |
| 07392532215896 | ANKYLOS® | 31021647 | 31021647 | 2020-11-18 |
| 07392532215988 | ANKYLOS® | 31021660 | 31021660 | 2020-11-18 |
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