Stent Tray 6900-21
by Mizuho Orthopedic Systems, Inc.
Stent Tray 6900-21 is a Class I device made by Mizuho Orthopedic Systems, Inc., listed in FDA GUDID since 30 Jun 2017 (UDI-DI 00842430100086), 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 | Number00842430100086 | Date30 Jun 2017 | StatusListed |
Official records
- AccessGUDID record 00842430100086
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Stent Tray
- Generic name
- Instrument table
- Model / Ref / Catalog
- 6900-21
- Primary DI / UDI-DI
- 00842430100086
- FDA product code
- FQO
- GMDN term
- Instrument table
- Device class
- Class I
- Regulation number
- 878.4960
- GUDID distribution status
- In Commercial Distribution
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