TiMesh®
- Primary DI
- 00721902805486
- Brand
- TiMesh®
- Company
- MEDTRONIC PS MEDICAL, INC.
- Model
- 8004105
- Device description
- BATTERY 8004105 BPD 5-PACK
- Published
- 2015-07-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HWC | Screw, fixation, bone |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K062348 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00721902805486 | Package | GS1 | 5 | In Commercial Distribution |
| 70721902805485 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00721902805486 | 00721902805486 | 721902805486 | 0721902805486 |
| 70721902805485 | 70721902805485 |
GMDN Terms#
| Term | Definition |
|---|---|
| Disposable battery pack | A group of battery cells (e.g., lithium ion cells) held within a container that is sterile used to provide temporary electrical energy to operate a medical device, typically when it is not possible, intentional, or convenient to connect the device being powered to a mains electricity (AC-powered) electrical outlet. This device is typically designed to power cordless surgical power tools (e.g., a non-rechargeable battery-powered surgical drilling system handpiece) and is non-rechargeable. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 089055867
- 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
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00763000029449 | N/A | 8023 B | 2020-03-07 | |
| 00763000030827 | N/A | 25077 | 2020-03-08 | |
| 00643169483316 | NA | 8023 B | 2015-06-24 | |
| 00643169498365 | NA | 25077 | 2015-07-14 | |
| 00643169507517 | NA | 8023 A | 2015-06-25 | |
| 00643169073623 | NA | 25077 | 2015-06-25 | |
| 00643169466142 | N/A | 46141 | 2015-07-15 | |
| 00673978228969 | NA | 46422 | 2015-06-18 | |
| 00673978246017 | NA | 27297 | 2015-07-21 | |
| 00673978246031 | NA | 27302 | 2015-07-14 | |
| 20643169466122 | N/A | 46440 | 2015-07-15 | |
| 00763000422646 | StrataMR2 | 46955MR | 2026-03-13 | |
| 00763000422684 | StrataMR2 | 46957MR | 2026-03-13 | |
| 00673978226835 | NA | 8591-60 | 2015-11-25 | |
| 00643169497955 | Clear-Site® | 46918 | 2015-09-16 | |
| 00613994450661 | Clear-Site® | 46918 | 2015-07-16 | |
| 00763000422660 | StrataMR II | 46956MR | 2025-05-02 | |
| 00763000422653 | Valve, StrataMR II, Regular | 46965MR | 2025-01-23 | |
| 00763000422677 | Snap Shunt Assembly, StrataMR II, Regular | 46966MR | 2025-01-23 | |
| 00763000422691 | Unassembled Shunt Kit, StrataMR II, Regular | 46967MR | 2025-01-23 |
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| 00688346005523 | Fine Osteotomy System - Tibial plate | Laboratoires Bodycad Inc | HWC | 2026-08-03 |
| 00688346005554 | Fine Osteotomy System - Tibial plate | Laboratoires Bodycad Inc | HWC | 2026-08-03 |
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