GUDID 08717213010949

X-Ray Catheter no.1, 100 cm

Nucletron B.V.

Bronchial brachytherapy system applicator, remote-afterloading
Primary Device ID08717213010949
NIH Device Record Keye09101f1-af76-4160-8477-1ab6bc115d66
Commercial Distribution StatusIn Commercial Distribution
Version Model Number089401P01-01
Company DUNS415269930
Company NameNucletron B.V.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com
Phone+1(770)300-9725
Emailinfo.america@elekta.com

Device Dimensions

Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS108717213010949 [Direct Marking]
GS108717213041721 [Primary]

FDA Product Code

JAQSystem, applicator, radionuclide, remote-controlled

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


[08717213010949]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-06-10
Device Publish Date2016-09-10

Devices Manufactured by Nucletron B.V.

08717213057203 - Smit Sleeve2024-07-15 Sleeve CT/MR Intrauterine Tube
08717213057258 - Smit Sleeve2024-07-15 Smit Sleeve CT/MR, 4mm
08717213054363 - Luneray2022-11-23 Catheter 6F 50cm, needle 37mm R30mm
08717213054370 - Luneray2022-11-23 Catheter 6F 50cm, needle 47mm R45mm
08717213054387 - Luneray2022-11-23 Catheter 6F 50cm, needle 57mm R60mm
08717213054394 - Luneray2022-11-15 Catheter 6F 50cm, needle 67mm R75mm
08717213057760 - Esteya2022-08-24 Esteya
08717213056947 - NA2022-07-08 INSERTION TOOL

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.