Runthrough 25-9092
by Terumo Corp.
Runthrough 25-9092 (TW*JJ415Z) is a Class II device made by Terumo Corp., listed in FDA GUDID since 9 Sep 2016 (UDI-DI 04987350703781), registry data as of 22 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 | Number04987350703781 | Date9 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04987350703781
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Runthrough
- Generic name
- Coronary artery guidewire extension
- Model / Ref / Catalog
- 25-9092, TW*JJ415Z
- Primary DI / UDI-DI
- 04987350703781
- FDA product code
- DQX
- GMDN term
- Coronary artery guidewire extension
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Outer Diameter — 0.36 MillimeterLength — 150 Centimeter
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