8000-060-013
8000-060-013 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 8 Aug 2018 (UDI-DI 07613327413151), registry data as of 23 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 | Number07613327413151 | Date8 Aug 2018 | StatusListed |
Official records
- AccessGUDID record 07613327413151
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Optical surgical tracking system spatial marker connector
- Model / Ref / Catalog
- 8000-060-013
- Primary DI / UDI-DI
- 07613327413151
- FDA product code
- HAW, PGW
- GMDN term
- Optical surgical tracking system spatial marker connector
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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