FDA UDI In Commercial Distribution 🇺🇸 United States

MUPIT Applicator

DI: 08717213043077 · Model: 110069P01-01 · Nucletron B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
MUPIT Applicator
Primary DI
08717213043077
Version / Model
110069P01-01
Company Name
Nucletron B.V.
Labeler DUNS
415269930
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2017-05-25
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
3b04ae33-0101-4dbc-884d-ea81f38bd32c

Device Description

MUPIT Bolt M3 x 5mm

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
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
38436 General-purpose brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 08717213043077
Unit of Use 08717213043060

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
5 – 35 Degrees Celsius