Identity
- Trade Name
- LiquiPhil™ FDA UDI
- Generic Name
- Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
- Device Name
- Hollow Tumors, Spherical, Spherical, hollow tumor set of seven with one each of the following diameters: 1cm, 1.5cm, 2cm, 3cm, 4cm, 5cm and 6cm FDA UDI
- Model / Reference
- TLP131 FDA UDI
- Description
- Hollow Tumors, Spherical, Spherical, hollow tumor set of seven with one each of the following diameters: 1cm, 1.5cm, 2cm, 3cm, 4cm, 5cm and 6cm FDA UDI
Identifiers
- Catalog Number
- TLP131 FDA UDI
- Primary DI / UDI-DI
- 00812266030673 FDA UDI
- FDA Product Code
- IXG FDA UDI
- GMDN Term
- Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1950 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multi-modality therapeutic radiation phantom, anthropomorphic
LiquiPhil™ by Providus Holdings, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Providus Holdings, Inc.
Sources (1)
- FDA UDI 611714b0-cc3d-4c52-a2ca-c1137abfe36c 34 fields · synced May 30, 2026