FDA UDI In Commercial Distribution 🇺🇸 United States

Henschke Titanium Applicator

DI: 08717213039360 · Model: 110436P01-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Henschke Titanium Applicator
Primary DI
08717213039360
Version / Model
110436P01-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
4786df46-d6aa-4c8e-9ccf-6602127eb9cf

Device Description

Intrauterine Tube, 15 °

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
38409 Cervical/intrauterine brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Direct Marking 08717213029934
Primary 08717213039360

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151272 000

Device Sizes

Type Value Unit Text
Angle 15.0 degree
Device Size Text, specify