FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08717213043015 · Model: 089515P01-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
08717213043015
Version / Model
089515P01-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
9701f0ec-645a-45ce-9ab5-edf9ddf42a44

Device Description

X-Ray Catheter 150 cm (5)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JAQ System, applicator, radionuclide, remote-controlled

GMDN Terms

Code Name
40808 Radiological image marker, implantable

Identifiers

Type ID
Direct Marking 08717213011571
Primary 08717213043015

Customer Contacts

Device Sizes

Type Value Unit Text
Length 151.0 Centimeter