Swish® Precision IO Scan Adapter
- Primary DI
- 10841307124160
- Brand
- Swish® Precision IO Scan Adapter
- Company
- IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Model
- 9065-09PT
- Catalog number
- 9065-09PT
- Published
- 2019-09-18
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
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 |
|---|---|---|---|---|
| 10841307124160 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10841307124160 | 10841307124160 |
GMDN Terms
| Term | Definition |
|---|---|
| Dental guided surgery reference pin | A non-sterile device in the form of a metal rod designed for the fabrication of custom-made scan and surgical dental implant templates used by a dentist during the first stage of a guided dental implantation procedure (i.e., drilling of holes in the jawbone for implant placement/fixation). It is a cylindrical metal pin placed in the holes of the reference plate to form a link between the chairside cone beam computerized tomography (CBCT) scan and a coordinate system for dental laboratory fabrication of the scan template (used to scan the patient) and then the surgical dental implant template. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| 1-888-649-6425 | customerservice@implantdirect.com |
Regulatory Flags
- DUNS number
- 868856969
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- 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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