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Austar
FDA UDIClass II (US FDA UDI)
by Austar Hearing Science & Technology (Xiamen) Co., Ltd men) Co., Ltd.
Identity
- Trade Name
- AUSTAR FDA UDI
- Generic Name
- Air-conduction hearing aid, behind-the-ear FDA UDI
- Model / Reference
- FH209-B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06943786083352 FDA UDI
- FDA Product Code
- QUG FDA UDI
- GMDN Term
- Air-conduction hearing aid, behind-the-ear FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3305 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Austar by Austar Hearing Science & Technology (Xiamen) Co., Ltd men) Co., Ltd. — Class II — 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 II | Pending data |
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Manufacturer
Sources (1)
- FDA UDI 4ab1891a-fdd9-4970-b00e-a62255e102a8 33 fields · synced Jun 8, 2026