FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08717213052789 · Model: 189367P01-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
08717213052789
Version / Model
189367P01-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-19
Public Version
2
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
8bcd9443-4169-4db6-ac9c-1719ebaa345f

Device Description

Flexible Implant Tube Cutter

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
JAQ System, applicator, radionuclide, remote-controlled

GMDN Terms

Code Name
38436 General-purpose brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Direct Marking 08717213052772
Previous 08717213040021
Primary 08717213052789

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022635 000
K032372 000
K983338 000