FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08717213013988 · Model: 101012-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
NA
Primary DI
08717213013988
Version / Model
101012-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
5d586256-127b-41e3-9b5d-11b8e3e353ef

Device Description

Sterilization Cap Set

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
Yes
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
38407 Vaginal brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 08717213013988
Unit of Use 08717213023840

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080934 000
K091154 000
K111973 000
K132889 000
K983341 000