ANKYLOS®
- Primary DI
- 07392532219122
- Brand
- ANKYLOS®
- Company
- Dentsply Implants Manufacturing GmbH
- Model
- 31034090
- Catalog number
- 31034090
- Device description
- ATP-Punch
- Published
- 2022-07-14
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- false
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 |
|---|---|---|---|---|
| 07392532219122 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07392532219122 | 07392532219122 | 7392532219122 |
GMDN Terms#
| Term | Definition |
|---|---|
| Dental soft-tissue coring punch, reusable | A dental instrument designed to remove with precision a circular section of oral soft tissue (e.g., gum, palatal mucosa) during dental surgery, typically to allow access to a site for drilling and dental/orthodontic implant placement without the use of a scalpel. Sometimes referred to as a mucotome, it will typically be designed with a handle at the proximal end for manual operation or for mounting into a dental power tool (e.g., contra-angle low-speed drill handpiece), and have a cylindrical hollow tube-like head with a sharp cutting at the distal end. It is typically made of high-grade stainless steel. This is a reusable device. |
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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 07392532175138 | Bone Trap | 22179 | 22179 | 2022-07-14 |
| 07392532032349 | Bone Trap | 22179 | 22179 | 2026-10-16 |
| EFRI9000001041 | SYMBIOS® | 900000104 | 900000104 | 2017-06-30 |
| EFRI9000003041 | SYMBIOS® | 900000304 | 900000304 | 2017-06-30 |
| EFRI9200001041 | SYMBIOS® | 920000104 | 920000104 | 2017-06-30 |
| EFRI9300001041 | SYMBIOS® | 930000104 | 930000104 | 2017-06-30 |
| EFRI9300003041 | SYMBIOS® | 930000304 | 930000304 | 2017-06-30 |
| EFRI9400000541 | SYMBIOS® | 940000054 | 940000054 | 2017-06-30 |
| EFRI9400001041 | SYMBIOS® | 940000104 | 940000104 | 2017-06-30 |
| EFRI9400003041 | SYMBIOS® | 940000304 | 940000304 | 2017-06-30 |
| EFRI9700001041 | SYMBIOS® | 970000104 | 970000104 | 2017-06-30 |
| EFRI9700003041 | SYMBIOS® | 970000304 | 970000304 | 2017-06-30 |
| EFRIUS99U000102 | Symbios ™ | PepGen P-15 Particulate | US99U000102 | 2014-12-02 |
| ERFIUS930000104 | Symbios ™ | OsteoGraf/N 300 (250-420 microns) | US930000104 | 2014-12-02 |
| ERFIUS930000304 | Symbios ™ | OsteoGraf/N 300 (250-420 microns) | US930000304 | 2014-12-02 |
| ERFIUS970000104 | Symbios ™ | OsteoGraf/N 700 (420–1000 microns) | US970000104 | 2014-12-02 |
| ERFIUS970000304 | Symbios ™ | OsteoGraf/N 700 (420–1000 microns) | US970000304 | 2014-12-02 |
| ERFIUS99U00014 | Symbios ™ | PepGen P-15 Particulate | US99U000104 | 2014-12-02 |
| ERFIUS99U000302 | Symbios ™ | PepGen P-15 Particulate | US99U000302 | 2014-12-02 |
| ERFIUS99U100052 | Symbios ™ | PepGen P-15 Flow | US99U100052 | 2014-12-02 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 07899995226457 | SLEEVE FOR SURGICAL GUIDEØ5.1MM OPEN | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226464 | SLEEVE FOR SURGICAL GUIDE Ø5.1MM OPEN | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226471 | SLEEVE FOR SURGICAL GUIDE Ø3.9MM OPEN | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226488 | SLEEVE FOR SURGICAL GUIDE Ø3.9MM OPEN | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226495 | SLEEVE FOR SURGICAL GUIDE Ø5.1MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226501 | SLEEVE FOR SURGICAL GUIDE Ø5.1MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226518 | SLEEVE FOR SURGICAL GUIDE Ø3.9MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226525 | SLEEVE FOR SURGICAL GUIDE Ø3.9MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226532 | SLEEVE FOR FIXER GUIDE Ø2.0MM PALATAL | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226556 | SLEEVE FOR FIXER GUIDE Ø2.0MM PALATAL | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995226563 | SLEEVE FOR FIXER GUIDE Ø1.4MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234346 | DRIVER RATCHET IMP. MT16° GUIDED | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234353 | DRIVER RATCHET IMP. MT16° GUIDED NARROW | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234360 | DRIVER HANDP. IMP. MT16° GUIDED | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234377 | DRIVER HANDP. IMP. MT16° GUIDED NARROW | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234391 | ANALOG REVERSE MICRO MINI ABUT. | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234407 | ANALOG REVERSE MINI ABUT. | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234414 | ANALOG REVERSE CM11.5° | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234421 | ANALOG REVERSE MT16° | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234438 | ANALOG REVERSE ABUT MULT. | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234445 | ANALOG HYBRIDO ABUT UNIV Ø4.5X6MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234452 | ANALOG HYBRIDO ABUT UNIV Ø4.5X4MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234469 | ANALOG HYBRIDO ABUT UNIV Ø3.3X6MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234476 | ANALOG HYBRIDO ABUT UNIV Ø3.3X4MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234490 | ANALOG HYBRID MICRO MINI ABUT. | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234506 | ANALOG HYBRID 4.5IH | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234513 | ANALOG HYBRID 3.5IH | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234520 | ANALOG HYBRID 3.0IH | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234537 | ANALOG HYBRID HI Ø4.5MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |
| 07899995234544 | ANALOG HYBRID HI Ø3.8MM | Sin Sistema de Implante Nacional S/A | NDP | 2026-10-29 |