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Avalon Biomed NeoSEALER Flo 10 Flex Flo Tips (Int'l)
FDA UDIClass I (US FDA UDI)
by Nusmile, Ltd
Identity
- Trade Name
- Avalon Biomed NeoSEALER Flo 10 Flex Flo Tips (Int'l) FDA UDI
- Generic Name
- Dental material injection cannula, single-use FDA UDI
- Device Name
- Avalon Biomed NeoSEALER Flo 10 Flex Flo Tips (Int'l) FDA UDI
- Model / Reference
- FFT10 FDA UDI
- Description
- Avalon Biomed NeoSEALER Flo 10 Flex Flo Tips (Int'l) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850008515262 FDA UDI
- FDA Product Code
- EIC FDA UDI
- GMDN Term
- Dental material injection cannula, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Avalon Biomed NeoSEALER Flo 10 Flex Flo Tips (Int'l) by Nusmile, Ltd — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Nusmile, Ltd
Sources (1)
- FDA UDI 23323a04-b07c-499a-9bf3-ecde56745ec5 34 fields · synced May 30, 2026