Hopkins 28132CA
Hopkins 28132CA is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551094464), 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 | Number04048551094464 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04048551094464
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Hopkins
- Generic name
- Rigid optical intracranial/spinal endoscope, reusable
- Model / reference
- 28132CA
- Primary DI / UDI-DI
- 04048551094464
- FDA product code
- GWG
- GMDN term
- Rigid optical intracranial/spinal endoscope, reusable
- Device class
- Class II
- Regulation number
- 882.1480
- GUDID distribution status
- In Commercial Distribution
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