Aesculap FV037T
by Christoph Miethke GmbH & Co. KG
Aesculap FV037T is a Class II device made by Christoph Miethke GmbH & Co. KG, listed in FDA GUDID since 24 Sep 2015 (UDI-DI 04041906117801), 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 | Number04041906117801 | Date24 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 04041906117801
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aesculap
- Generic name
- Cranial port/reservoir
- Model / Ref / Catalog
- FV037T
- Primary DI / UDI-DI
- 04041906117801
- FDA product code
- JXG
- GMDN term
- Cranial port/reservoir
- Device class
- Class II
- Regulation number
- 882.5550
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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