NAVIGATOR®
- Primary DI
- 00844868024163
- Brand
- NAVIGATOR®
- Company
- BIOMET 3I, LLC
- Model
- SGTCP4L
- Device description
- TAPERED NAVIGATOR® CORTICAL PERFORATOR 4.1MM(D) LONG
- Published
- 2016-03-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
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 |
|---|---|---|---|---|
| 00844868024163 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00844868024163 | 00844868024163 | 844868024163 | 0844868024163 |
GMDN Terms
| Term | Definition |
|---|---|
| Fixture/appliance dental drill bit, reusable | A shaft of metal intended to be used in dental surgery to create channels of appropriate depth and diameter in bone (osteotomy) of the oral cavity to facilitate the implantation of a dental fixture/appliance. The device is typically available in a set of graduated sizes and various forms and functions (e.g., guide, pilot, twist, cortical, conical). It is attached to a manual or power tool handpiece that provides rotation. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)342-5454 | 3iPBG-CS@biomet.com |
Regulatory Flags
- DUNS number
- 186127825
- 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
- true
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|---|---|---|---|---|
| 00844868051824 | Single Patient ACT® Twist Drill | SPACT2015 | 2025-12-18 | |
| 00844868051831 | Single Patient ACT® Twist Drill, 2mmD x 10mmL | SPACT2010 | 2025-12-18 | |
| 00844868051848 | Single Patient ACT® Twist Drill | SPACT2020 | 2025-12-18 | |
| 00844868051855 | Single Patient ACT® Twist Drill | SPACT206S | 2025-12-18 | |
| 00844868051862 | Single Patient ACT® Twist Drill | SPACT2710 | 2025-12-18 | |
| 00844868051879 | Single Patient ACT® Twist Drill | SPACT2715 | 2025-12-18 | |
| 00844868051886 | Single Patient ACT® Twist Drill | SPACT2720 | 2025-12-18 | |
| 00844868051893 | Single Patient ACT® Twist Drill | SPACT3010 | 2025-12-18 | |
| 00844868051909 | Single Patient ACT® Twist Drill | SPACT3015 | 2025-12-18 | |
| 00844868051916 | Single Patient ACT® Twist Drill | SPACT3020 | 2025-12-18 | |
| 00844868051923 | Single Patient ACT® Twist Drill | SPACT3110 | 2025-12-18 | |
| 00844868051930 | Single Patient ACT® Twist Drill | SPACT3115 | 2025-12-18 | |
| 00844868051947 | Single Patient ACT® Twist Drill | SPACT3120 | 2025-12-18 | |
| 00844868051954 | Single Patient ACT® Twist Drill | SPACT3210 | 2025-12-18 | |
| 00844868051961 | Single Patient ACT® Twist Drill | SPACT3215 | 2025-12-18 | |
| 00844868051978 | Single Patient ACT® Twist Drill | SPACT3220 | 2025-12-18 | |
| 00844868051985 | Single Patient ACT® Twist Drill | SPACT326S | 2025-12-18 | |
| 00844868051992 | Single Patient ACT® Twist Drill | SPACT3810 | 2025-12-18 | |
| 00844868052005 | Single Patient ACT® Twist Drill | SPACT3815 | 2025-12-18 | |
| 00844868052012 | Single Patient ACT® Twist Drill | SPACT3820 | 2025-12-18 |
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