Identity
- Trade Name
- Interacoustics FDA UDI
- Generic Name
- Canalith repositioning procedure chair, manual FDA UDI
- Model / Reference
- TRV FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05711117219098 FDA UDI
- FDA Product Code
- LXV FDA UDI
- GMDN Term
- Canalith repositioning procedure chair, manual FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Canalith repositioning procedure chair, manual
Interacoustics by Interacoustics A/S — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Interacoustics A/S
Sources (1)
- FDA UDI fa4755d2-8f87-44aa-a6c3-2fb3798045c4 32 fields · synced May 30, 2026