FDA UDI In Commercial Distribution 🇺🇸 United States

Interstitial needles

DI: 08717213052154 · Model: 083250P02-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Interstitial needles
Primary DI
08717213052154
Version / Model
083250P02-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-02-18
Public Version
5
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
1f85dda6-bc4c-4fe5-be62-14ba84bf4c30

Device Description

Obturator for 1.9mm Needle x 80mm

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
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 08717213007307
Primary 08717213052154
Unit of Use 88717213007303

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091154 000

Device Sizes

Type Value Unit Text
Device Size Text, specify
Length 80.0 Millimeter
Outer Diameter 1.9 Millimeter