FDA UDI In Commercial Distribution 🇺🇸 United States

Utrecht Interstitial Fletcher CT/MR Applicator

DI: 08717213034945 · Model: 110369-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Utrecht Interstitial Fletcher CT/MR Applicator
Primary DI
08717213034945
Version / Model
110369-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-24
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
47e6028c-ec2c-4cd6-b0be-73af4bfd80d4

Device Description

Interstitial Ovoid (left) 25mm 15°, R12,5

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 Safe
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
38409 Cervical/intrauterine brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 08717213034945

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091154 000

Device Sizes

Type Value Unit Text
Width 25.0 Millimeter
Device Size Text, specify Radius 12.5mm
Angle 15.0 degree

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 90 Percent (%) Relative Humidity