Olympus WA90004W
Olympus WA90004W is a medical device (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Olympus Winter & Ibe GmbH, listed in FDA GUDID since 31 Jul 2020 (UDI-DI 04042761083560), 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 | Number04042761083560 | Date31 Jul 2020 | StatusListed |
Official records
- AccessGUDID record 04042761083560
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Olympus
- Generic name
- Argon-enhanced electrosurgical system gas delivery unit
- Model / Ref / Catalog
- WA90004W
- Primary DI / UDI-DI
- 04042761083560
- FDA product code
- GEI
- GMDN term
- Argon-enhanced electrosurgical system gas delivery unit
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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