Msi 742-02
by Modern Surgical Instruments LLC
Msi 742-02 is a Class I device made by Modern Surgical Instruments LLC, listed in FDA GUDID since 30 Mar 2023 (UDI-DI 00810130201853), 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 | Number00810130201853 | Date30 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 00810130201853
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Msi
- Generic name
- Orthopaedic surgical distractor, external
- Model / reference
- 742-02
- Primary DI / UDI-DI
- 00810130201853
- FDA product code
- GAD
- GMDN term
- Orthopaedic surgical distractor, external
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code GAD (Retractor).
- Gimmi AD.1752.10 by Gimmi GmbH
- BENT HOHMAN RETRACTORS 2142-75-000 214275000 by Biomet Orthopedics, Inc.
- LANDANGER B80550 by LANDANGER
- Omni-Tract® 11442 by Integra Lifesciences Corp.
- 4033-43-01 00-4033-043-01 by Zimmer, Inc.
- Omni-Tract® 3806R by Integra Lifesciences Corp.
- LANDANGER B80720 by LANDANGER
- MicroFrance® CP23-8 by Integra Microfrance
- SCANLAN® Retractor 8008-43-1R by SCANLAN INTERNATIONAL INC
- CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000 by Clarus Medical Systems, Inc.