Parallel Wire Guide, for φ2.5 Guide Wire, Adjustable 110200600
by Double Medical Technology Inc.
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06902139111258 | Date1 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK130108 | Date19 Apr 2013 | StatusActive |
Official records
- AccessGUDID record 06902139111258
- FDA 510(k) database K130108
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Parallel Wire Guide, for φ2.5 Guide Wire, Adjustable
- Generic name
- Orthopaedic guidewire, reusable
- Model / Ref / Catalog
- 110200600
- Primary DI / UDI-DI
- 06902139111258
- 510(k) Number
- FDA product code
- HWC, HRS
- GMDN term
- Orthopaedic guidewire, reusable
- Device class
- Class II
- Regulation number
- 888.3040, 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from Double Medical Technology Inc.
Properties
Other properties (12)
- Supplied sterile: No
- Single use: No
- Implantable: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No
- Manufacturing date: No