FDA UDI In Commercial Distribution 🇺🇸 United States

LiquiPhil™

DI: 00812266030772 · Model: TLP260 · Providus Holdings, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LiquiPhil™
Primary DI
00812266030772
Version / Model
TLP260
Catalog Number
TLP260
Company Name
Providus Holdings, Inc.
Labeler DUNS
104162493
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-07
Public Version
1
Public Version Date
2024-05-15
Public Version Status
New
Public Device Record Key
8c583459-52ab-4388-b818-ab253d3993cc

Device Description

LiquiPhil™ End-to-End Pelvis, includes pelvis form, two 10cm ovoid tumor vessels and permanent storage case

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IXG Phantom, Anthropomorphic, Radiographic

GMDN Terms

Code Name
40631 Multi-modality therapeutic radiation phantom, test object
40636 MRI phantom, test object

Identifiers

Type ID
Primary 00812266030772