FDA UDI In Commercial Distribution 🇺🇸 United States

Delta4 Phantom+

DI: 17350005180024 · Model: Wired (PMMA) · Scandidos AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Delta4 Phantom+
Primary DI
17350005180024
Version / Model
Wired (PMMA)
Catalog Number
SDOS101-35
Company Name
Scandidos AB
Labeler DUNS
507639297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ff1024d4-87af-41e6-86f1-8f982f583769

Device Description

The intended use of the device is • quality assurance of patient specific treatment delivery prior to the treatment in IMRT (including VMAT) and 4DRT (e.g. respiratory gating and tumour tracking). • quality assurance of the radiation delivery system.

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
40624 Multi-modality therapeutic radiation phantom, anthropomorphic

Identifiers

Type ID
Primary 17350005180024

Customer Contacts

Phone
+46184723030