FDA UDI
In Commercial Distribution
🇺🇸 United States
Amplivox
DI: 05060488902680
·
Model: Otowave 302+
·
AMPLIVOX LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Amplivox
- Primary DI
- 05060488902680
- Version / Model
- Otowave 302+
- Company Name
- AMPLIVOX LIMITED
- Labeler DUNS
- 226599157
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-12-22
- Public Version
- 1
- Public Version Date
- 2024-01-01
- Public Version Status
- New
- Public Device Record Key
- 103654d8-a3fc-403c-8813-6fbfc9934763
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| ETY | Tester, Auditory Impedance | Ear, Nose, Throat | 874.1090 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 63545 | Vestibulo-auditory analysis system | An assembly of devices designed to assess the function of the auditory and vestibular systems using multiple vestibulo-auditory parameters which include audiometry (e.g., air, bone, speech), tympanometry, auditory evoked-potential (AEP) [e.g., auditory brainstem response (ABR)], otoacoustic emission (OAE), auditory steady-state response (ASSR), and vestibular evoked myogenic potential (VEMP). It includes a console which may be connected to an off-the-shelf computer, devices used for the transmission of stimuli and reception of electrical signals generated by the patient (e.g., preamplifier, audiometric ear tips, electrodes), and dedicated software. This is a reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 05060488902680 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K171265 | 000 |