FDA UDI In Commercial Distribution 🇺🇸 United States

ProGuide Needles

DI: 08717213025103 · Model: 189652-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
6

Basic Information

Brand Name
ProGuide Needles
Primary DI
08717213025103
Version / Model
189652-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2016-09-10
Public Version
5
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
7714b0b3-ba7f-4031-bb49-b9e9ebd28b04

Device Description

ProGuide Obturator 6Fx240 mm

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
Yes
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 08717213025110
Package 08717213025448
Primary 08717213025103
Unit of Use 88717213025116

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060349 000

Device Sizes

Type Value Unit Text
Length 240.0 Millimeter
Catheter Gauge 6.0 French