egger flex/AB 40 shore, pink
by egger Otoplastik + Labortechnik GmbH GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberEGOL208351 | Date31 Aug 2022 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- egger
- Generic Name
- Earmould, custom-made
- Model / Reference
- flex/AB 40 shore, pink
- Primary DI / UDI-DI
- EGOL208351
- FDA Product Code
- ESD
- GMDN Term
- Earmould, custom-made
- Device Class
- Class I
- Regulation Number
- 874.3300
- Commercial Distribution
- Not in Commercial Distribution
Other devices from egger Otoplastik + Labortechnik GmbH
Properties
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No