Tunneler L
- Primary DI
- 04035479170295
- Brand
- Tunneler L
- Company
- BIOTRONIK SE & Co. KG
- Model
- 457856
- Catalog number
- 457856
- Published
- 2026-05-28
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| LGW | Stimulator, spinal-cord, totally implanted for pain relief |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief | Unknown | 3 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| P210037 | 012 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04035479170295 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04035479170295 | 04035479170295 | 4035479170295 |
GMDN Terms#
| Term | Definition |
|---|---|
| Subcutaneous tunneller, single-use | A hand-held manual surgical instrument designed to create a subcutaneous tunnel (artificial passageway) between percutaneous entry and exit incisions for the subcutaneous placement of a device (e.g., catheter for medication administration, shunt). It is available in a variety of forms and may be: 1) a luminal sheath with a removable inner obturator, intended for co-axial device introduction, followed by sheath removal; or 2) a non-luminal device intended to either lead or pull the device through subcutaneous tissue. It is not intended for tunnelling through deep tissues and is not a dedicated pacing or defibrillation lead tunneller. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 | 0 |
Contacts#
| Phone | |
|---|---|
| +1(888)345-0374 | jon.brumbaugh@biotronik.com |
Regulatory Flags#
- DUNS number
- 315620229
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 04035479162061 | Selectra 3D-40-39 | 443625 | 443625 | 2020-11-12 |
| 04035479162078 | Selectra 3D-55-32 | 443626 | 443626 | 2020-11-12 |
| 04035479162085 | Selectra 3D-55-39 | 443627 | 443627 | 2020-11-12 |
| 04035479162092 | Selectra 3D-65-32 | 443628 | 443628 | 2020-11-12 |
| 04035479162108 | Selectra 3D-65-39 | 443629 | 443629 | 2020-11-12 |
| 07640130455399 | Selectra | 3D-40-42 | 451789 | 2020-11-12 |
| 07640130455405 | Selectra | 3D-55-42 | 451790 | 2020-11-12 |
| 07640130455412 | Selectra | 3D-65-42 | 451791 | 2020-11-12 |
| 04035479176228 | Selectra 3D-65-42 | 451791 | 451791 | 2021-06-02 |
| 04035479176235 | Selectra 3D-55-42 | 451790 | 451790 | 2021-06-02 |
| 04035479176242 | Selectra 3D-40-42 | 451789 | 451789 | 2021-06-02 |
| 04035479116828 | Selectra | IC-50-65 | 375545 | 2014-08-27 |
| 04035479116835 | Selectra | IC-50-75 | 375546 | 2014-08-27 |
| 04035479116842 | Selectra | IC-90-65 | 375547 | 2014-08-27 |
| 04035479116859 | Selectra | IC-90-75 | 375548 | 2014-08-27 |
| 04035479116651 | Selectra Amplatz 6.0-45 | 375519 | 375519 | 2014-08-27 |
| 04035479116668 | Selectra Amplatz 6.0-55 | 375520 | 375520 | 2014-08-27 |
| 04035479116675 | Selectra BIO2-45 | 375523 | 375523 | 2014-08-27 |
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