NA
- Primary DI
- 07611819083417
- Brand
- NA
- Company
- SYNTHES (U.S.A.) LP
- Model
- 357.516
- Catalog number
- 357516
- Device description
- CANNULATED SHAFT 8MM HEX FOR TI FEMORAL NAILS
- Published
- 2016-12-31
- 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 |
|---|---|
| HXC | WRENCH |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HXC | Wrench | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07611819083417 | Direct Marking | GS1 | 0 | |
| 10886982196521 | Primary | GS1 | 0 | |
| H6793575160 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07611819083417 | 07611819083417 | 7611819083417 |
| 10886982196521 | 10886982196521 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical screwdriver, reusable | A non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags
- DUNS number
- 832637081
- 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
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| H981PDL432F | NA | PDL432 | PDL432 | 2017-02-20 |
| H981PDL434H | NA | PDL434 | PDL434 | 2017-02-20 |
| 07611819995796 | NA | 03.820.144 | 03820144 | 2016-12-31 |
| 07611819943490 | NA | E5115-7 | E51157 | 2017-02-20 |
| H679E51157P09 | NA | E5115-7P | E51157P | 2016-12-31 |
| 10886982293060 | NA | 04.045.260 | 04045260 | 2025-01-31 |
| 10886982293237 | NA | 04.045.230 | 04045230 | 2025-01-31 |
| 10886982293244 | NA | 04.045.232 | 04045232 | 2025-01-31 |
| 10886982293251 | NA | 04.045.234 | 04045234 | 2025-01-31 |
| 10886982293268 | NA | 04.045.236 | 04045236 | 2025-01-31 |
| 10886982293275 | NA | 04.045.238 | 04045238 | 2025-01-31 |
| 10886982293282 | NA | 04.045.240 | 04045240 | 2025-01-31 |
| 10886982293299 | NA | 04.045.242 | 04045242 | 2025-01-31 |
| 10886982293305 | NA | 04.045.244 | 04045244 | 2025-01-31 |
| 10886982293312 | NA | 04.045.246 | 04045246 | 2025-01-31 |
| 10886982293329 | NA | 04.045.248 | 04045248 | 2025-01-31 |
| 10886982293336 | NA | 04.045.250 | 04045250 | 2025-01-31 |
| 10886982293343 | NA | 04.045.252 | 04045252 | 2025-01-31 |
| 10886982293350 | NA | 04.045.254 | 04045254 | 2025-01-31 |
| 10886982293367 | NA | 04.045.256 | 04045256 | 2025-01-31 |
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