N/A
- Primary DI
- 00643169097889
- Brand
- N/A
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- A07A
- Device description
- MIXER A07A CEMENT
- Published
- 2021-10-03
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| JDZ | MIXER, CEMENT, FOR CLINICAL USE |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| JDZ | Mixer, Cement, For Clinical Use | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00643169097889 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00643169097889 | 00643169097889 | 643169097889 | 0643169097889 |
GMDN Terms
| Term | Definition |
|---|---|
| Manual orthopaedic cement mixer, reusable | A hand-operated manual device designed to mix polymethylmethacrylate (PMMA) powder with methylmethacrylate monomer in order to produce polymerizing bone cement. It typically includes a single-use inner mixing bowl where the cement is mixed, an outer housing with a handcrank and driving gears connected to a disposable mixing blade(s), and a lid. The device is intended to be connected to, or placed under, a fume extraction device to prevent fumes from polluting the working environment; it is typically operated outside of the sterile surgical field. This is a reusable device. |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags
- DUNS number
- 830350380
- 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
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