FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08717213024403 · Model: 189894-00 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
08717213024403
Version / Model
189894-00
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-10-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
99a5fedf-133f-4ef5-9182-b2419dc92214

Device Description

Fixation Screw Set (Ovoid, Stopper)

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

Identifiers

Type ID
Primary 08717213024403
Unit of Use 88717213024403

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091154 000
K132889 000
K151272 000
K983341 000