Rps 8800004000
Rps 8800004000 (8800-004-000) is an electrical-only medical device connection cable (FDA Class II; FDA product code OLO, Orthopedic stereotaxic instrument) made by Stryker Corp., listed in FDA GUDID since 1 Oct 2025 (UDI-DI 07613327631760), 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 | Number07613327631760 | Date1 Oct 2025 | StatusListed |
Official records
- AccessGUDID record 07613327631760
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rps
- Generic name
- Electrical-only medical device connection cable, reusable
- Model / Ref / Catalog
- 8800004000, 8800-004-000
- Primary DI / UDI-DI
- 07613327631760
- FDA product code
- OLO
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code OLO (Orthopedic stereotaxic instrument).
- DeGen Navigated Instrumentation by Degen Medical
- CD HORIZON® Spinal System RBT023302 by MEDTRONIC SOFAMOR DANEK, INC.
- OMNIBotics NV-LPT02 by OMNIlife science, Inc.
- Spine Guidance Software, Stryker Q Guidance System by Stryker Leibinger GmbH & Co.KG
- V40 110765 by MAKO Surgical Corp.
- OMNIBotics NS-5036B by OMNIlife science, Inc.
- 6002-140-000 by Stryker Leibinger
- 6003-010-000 by Stryker Leibinger
- TMINI™ Miniature Robotic System by Think Surgical Inc.
- Joimax® Intracs® EM Patient Tracker JINTPT2235 by Joimax GmbH