Aesculap PE204RE
by Aesculap AG
Aesculap PE204RE is a Class II device made by Aesculap AG, listed in FDA GUDID since 6 Feb 2017 (UDI-DI 04038653416721), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04038653416721 | Date6 Feb 2017 | StatusListed |
Official records
- AccessGUDID record 04038653416721
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aesculap
- Generic name
- Rigid optical intracranial/spinal endoscope, reusable
- Model / Ref / Catalog
- PE204RE
- Primary DI / UDI-DI
- 04038653416721
- 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
- Sterilisation method
- Moist Heat or Steam Sterilization
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