FDA UDI In Commercial Distribution 🇺🇸 United States

ProGuide Needles

DI: 08717213025202 · Model: 110233-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ProGuide Needles
Primary DI
08717213025202
Version / Model
110233-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-25
Public Version
5
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
1623d3cb-db77-4594-aa7f-daee60cace2d

Device Description

ProGuide Round Needle 6Fx294mm

Device Characteristics

Single Use
Yes
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 Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

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
Package 08717213021204
Primary 08717213025202

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060349 000
K091154 000

Device Sizes

Type Value Unit Text
Catheter Gauge 6.0 French
Length 294.0 Millimeter
Device Size Text, specify