FDA UDI In Commercial Distribution 🇺🇸 United States

Geneva

DI: 08717213056572 · Model: 152020-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Geneva
Primary DI
08717213056572
Version / Model
152020-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-14
Public Version
1
Public Version Date
2020-08-24
Public Version Status
New
Public Device Record Key
7cb5fda6-436c-40c5-a2f2-133266cb994a

Device Description

Intrauterine Tube 40mm 45°

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 Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 08717213056565
Primary 08717213056572

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201272 000

Device Sizes

Type Value Unit Text
Angle 45.0 degree