VITALITY®+ POWER
- Primary DI
- 00880304855045
- Brand
- VITALITY®+ POWER
- Company
- BIOMET SPINE LLC
- Model
- 731M0030
- Catalog number
- 731M0030
- Published
- 2017-12-12
- 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
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 |
|---|
| 00880304855045 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00880304855045 | 00880304855045 | 880304855045 | 0880304855045 |
GMDN Terms
| Term | Definition |
|---|
| Fluted surgical drill bit, reusable | A shaft of metal with an obtuse, V-shaped cutting edge designed to be rotated to bore into bone to create a hole of the same dimension as the diameter of the shaft. This device, commonly called a "twist drill", has a cylindrical design with a double-edged cutting head that is formed from two spiralled flutes that extend the length of the insertion part of the drill. At the proximal end, it is usually inserted into a surgical power tool or a surgical hand drill/brace. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 018577570
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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 |
|---|
| 00763000817305 | VERTEX® Reconstruction System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-03-16 |
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