7325122
7325122 (7325.122) is a Class II device made by Richard Wolf GmbH, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207013717), 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 | Number04055207013717 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04055207013717
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Flexible fibreoptic hysteroscope
- Model / Ref / Catalog
- 7325122, 7325.122
- Primary DI / UDI-DI
- 04055207013717
- FDA product code
- HRX
- GMDN term
- Flexible fibreoptic hysteroscope
- Device class
- Class II
- Regulation number
- 888.1100
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Hydrogen Peroxide
- Size
- Length — 200 MillimeterOuter Diameter — 2.5 Millimeter
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