Mini Step MS101003
by Covidien LP
Mini Step MS101003 is a Class II device made by Covidien LP, cleared under FDA 510(k) K961430 on 28 May 1996 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20884521082721), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20884521082721 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK961430 | Date28 May 1996 | StatusActive |
Official records
- AccessGUDID record 20884521082721
- FDA 510(k) database K961430
Across registries
- FDA 510(k) K961430 decided 28 May 1996 Active
- FDA GUDID UDI-DI 20884521082721 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K961430
- Listed FDA GUDID 20884521082721
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mini Step
- Generic name
- Laparoscopic multi-instrument access port, single-use
- Model / reference
- MS101003
- Primary DI / UDI-DI
- 20884521082721
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Laparoscopic multi-instrument access port, single-use
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 3 MillimeterOuter Diameter — 2 Millimeter
Similar devices in this category
Other devices filed under Laparoscopic multi-instrument access port, single-use.