Dextrus 4135
Dextrus 4135 (358744) is a Class III device made by BIOTRONIK SE & Co. KG, listed in FDA GUDID since 30 Sep 2015 (UDI-DI 04035479143206), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04035479143206 | Date30 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 04035479143206
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dextrus
- Generic name
- Endocardial/interventricular septal pacing lead
- Model / Ref / Catalog
- 4135, 358744
- Primary DI / UDI-DI
- 04035479143206
- FDA product code
- NVN
- GMDN term
- Endocardial/interventricular septal pacing lead
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
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