Identity
- Trade Name
- Bioseal Inc. FDA UDI
- Generic Name
- Assistive liquid funnel FDA UDI
- Device Name
- Funnel 2 3/4" Diameter FDA UDI
- Model / Reference
- 19015/25 FDA UDI
- Description
- Funnel 2 3/4" Diameter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00630094190150 FDA UDI
- FDA Product Code
- KDC FDA UDI
- GMDN Term
- Assistive liquid funnel FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Category: Assistive liquid funnel
Bioseal Inc. by Bioseal — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bioseal
Sources (1)
- FDA UDI 3a1d101e-d6b3-40e4-8e32-5d5df9a56eb9 33 fields · synced Jun 8, 2026