N/A
- Primary DI
- 00643169589896
- Brand
- N/A
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 7372572
- Device description
- TEMPLATE 7372572 72.5MM PLATE TEMPLATE
- Published
- 2019-03-08
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00643169589896 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00643169589896 | 00643169589896 | 643169589896 | 0643169589896 |
GMDN Terms
| Term | Definition |
|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Length | 72.5 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 830350380
- Device count
- 1
- DM exempt
- true
- 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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| Primary DI | Brand | Company | Product code | Published |
|---|
| 04052536216710 | neon3 | Ulrich GmbH & Co. KG | KWP | 2026-05-26 |
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| 00763000817312 | VERTEX® Reconstruction System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-03-16 |
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