FDA UDI In Commercial Distribution 🇺🇸 United States

Advanced Gynecological Applicator

DI: 08717213053649 · Model: 126050-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Advanced Gynecological Applicator
Primary DI
08717213053649
Version / Model
126050-01
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
ad92dcc6-bb67-4414-9e81-7c8c3a1fa440

Device Description

Guiding Tube For Interstitial Lunar Ovoid Tube

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 08717213054134
Primary 08717213053649

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161688 000