Aurical 8-04-14530-CA
Aurical 8-04-14530-CA is a Class II device made by Natus Medical Denmark ApS, listed in FDA GUDID since 1 Jul 2021 (UDI-DI 05713315009211), 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 | Number05713315009211 | Date1 Jul 2021 | StatusListed |
Official records
- AccessGUDID record 05713315009211
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aurical
- Generic name
- Speech audiometer
- Model / Ref / Catalog
- 8-04-14530-CA
- Primary DI / UDI-DI
- 05713315009211
- FDA product code
- EWO
- GMDN term
- Speech audiometer
- Device class
- Class II
- Regulation number
- 874.1050
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code EWO (Audiometer).
- SIBELMED AC50D by Trutone
- AUTOMATIC SELF-OPERATED SCREENING AUDIOMETER DEVICE (ASAM) by Bar - Advanced Control Systems, Ltd.
- TYPE FA10 AUDIOMETER by FRYE ELECTRONICS, INC.
- MODEL V4 AUDIOMETER by Digital Hearing Systems Corp.
- AUDIOSCREENER OAE by Kedly, Inc.
- AUDIOMETER MODEL MD-4, MD-4P by Singer Medical Products, Inc.
- AMPLAID A311 SERIES by Amplifon S.p.A
- ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER by Ethical Hearing Instruments
- AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM by Bio-Logic Systems Corp.
- THE MAX SYSTEM, MODEL: BASIC, 1000, 2000 AUDIOMETER by Sound Linked Data, Inc.