FDA UDI Not in Commercial Distribution 🇺🇸 United States

Interstitial needles

DI: 08717213051812 · Model: 089007P02-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Interstitial needles
Primary DI
08717213051812
Version / Model
089007P02-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2017-01-14
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
c3e7e9ee-8728-4700-b851-de6cf94a5727
Distribution End Date
2017-02-21

Device Description

Obturator for 1.5mm Needle x 140mm

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
MR Unsafe
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
38436 General-purpose brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Direct Marking 08717213009950
Primary 08717213051812
Unit of Use 88717213051812

Customer Contacts