FDA UDI In Commercial Distribution 🇺🇸 United States

Utrecht Interstitial Fletcher CT/MR Applicator

DI: 08717213053663 · Model: 110235-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Utrecht Interstitial Fletcher CT/MR Applicator
Primary DI
08717213053663
Version / Model
110235-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-26
Public Version
1
Public Version Date
2019-12-04
Public Version Status
New
Public Device Record Key
0b0bf6ae-0d72-4928-9c33-371b830fb6a6

Device Description

Guiding Tube for Ovoids

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
38409 Cervical/intrauterine brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Package 08717213054127
Primary 08717213053663

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091154 000