Aesculap US401
Aesculap US401 is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04046964583360), 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 | Number04046964583360 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04046964583360
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aesculap
- Generic name
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
- Model / Ref / Catalog
- US401
- Primary DI / UDI-DI
- 04046964583360
- FDA product code
- GEI
- GMDN term
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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